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- [1] A Novel Frameshift Mutation in the AFG3L2 Gene in a Patient with Spinocerebellar AtaxiaCEREBELLUM, 2014, 13 (03): : 331 - 337Musova, Zuzana论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech Republic Univ Hosp Motol, Prague, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicKaiserova, Michaela论文数: 0 引用数: 0 h-index: 0机构: Palacky Univ, Dept Neurol, Fac Med & Dent, CR-77147 Olomouc, Czech Republic Univ Hosp, Olomouc, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicKriegova, Eva论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp, Olomouc, Czech Republic Palacky Univ, Dept Immunol, Fac Med & Dent, CR-77147 Olomouc, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicFillerova, Regina论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp, Olomouc, Czech Republic Palacky Univ, Dept Immunol, Fac Med & Dent, CR-77147 Olomouc, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicVasovcak, Peter论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech Republic Univ Hosp Motol, Prague, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicSantava, Alena论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp, Olomouc, Czech Republic Palacky Univ, Dept Med Genet & Foetal Med, Fac Med & Dent, CR-77147 Olomouc, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicMensikova, Katerina论文数: 0 引用数: 0 h-index: 0机构: Palacky Univ, Dept Neurol, Fac Med & Dent, CR-77147 Olomouc, Czech Republic Univ Hosp, Olomouc, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicZumrova, Alena论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Motol, Prague, Czech Republic Charles Univ Prague, Dept Child Neurol, Fac Med 2, Prague, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicKrepelova, Anna论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech Republic Univ Hosp Motol, Prague, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicSedlacek, Zdenek论文数: 0 引用数: 0 h-index: 0机构: Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech Republic Univ Hosp Motol, Prague, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech RepublicKanovsky, Petr论文数: 0 引用数: 0 h-index: 0机构: Palacky Univ, Dept Neurol, Fac Med & Dent, CR-77147 Olomouc, Czech Republic Univ Hosp, Olomouc, Czech Republic Charles Univ Prague, Dept Biol & Med Genet, Fac Med 2, Prague, Czech Republic
- [2] A Novel Frameshift Mutation in the AFG3L2 Gene in a Patient with Spinocerebellar AtaxiaThe Cerebellum, 2014, 13 : 331 - 337Zuzana Musova论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsMichaela Kaiserova论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsEva Kriegova论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsRegina Fillerova论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsPeter Vasovcak论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsAlena Santava论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsKaterina Mensikova论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsAlena Zumrova论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsAnna Krepelova论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsZdenek Sedlacek论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical GeneticsPetr Kanovsky论文数: 0 引用数: 0 h-index: 0机构: Charles University 2nd Faculty of Medicine and University Hospital Motol,Department of Biology and Medical Genetics
- [3] Partial deletion of AFG3L2 causing spinocerebellar ataxia type 28NEUROLOGY, 2014, 82 (23) : 2092 - 2100Smets, Katrien论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neurogenet Lab, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neuropathol Lab, Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumDeconinck, Tine论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neurogenet Lab, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neuropathol Lab, Antwerp, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumBaets, Jonathan论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neurogenet Lab, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neuropathol Lab, Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumSieben, Anne论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Inst Born Bunge, Neurogenet Lab, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neuropathol Lab, Antwerp, Belgium Ghent Univ Hosp, Dept Neurol, Ghent, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumMartin, Jean-Jacques论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Inst Born Bunge, Neurogenet Lab, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neuropathol Lab, Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumSmouts, Iris论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumWang, Shuaiyu论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Bioctr, Cologne, Germany Cologne Excellence Cluster Cellular Stress Respon, Cologne, Germany Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumTaroni, Franco论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol Carlo Besta, Unit Genet Neurodegenerat & Metab Dis, Milan, Italy Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumDi Bella, Daniela论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol Carlo Besta, Unit Genet Neurodegenerat & Metab Dis, Milan, Italy Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumVan Hecke, Wim论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp Hosp, Dept Radiol, Antwerp, Belgium Icometrix, Leuven, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumParizel, Paul M.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp Hosp, Dept Radiol, Antwerp, Belgium Icometrix, Leuven, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumJadoul, Christina论文数: 0 引用数: 0 h-index: 0机构: AZ Nicolaas, Dept Neurol, St Niklaas, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumDe Potter, Robert论文数: 0 引用数: 0 h-index: 0机构: AZ Sint Lucas, Dept Neurol, Ghent, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, BelgiumCouvreur, Francine论文数: 0 引用数: 0 h-index: 0机构: AZ Klina, Dept Neurol, Brasschaat, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium论文数: 引用数: h-index:机构:De Jonghe, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neurogenet Lab, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neuropathol Lab, Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium Univ Antwerp, VIB Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium
- [4] A Novel Missense Mutation in AFG3L2 Associated with Late Onset and Slow Progression of Spinocerebellar Ataxia Type 28JOURNAL OF MOLECULAR NEUROSCIENCE, 2014, 52 (04) : 493 - 496Loebbe, Anna Mareike论文数: 0 引用数: 0 h-index: 0机构: Univ Giessen, Inst Humangenet, D-35392 Giessen, Germany Univ Giessen, Inst Humangenet, D-35392 Giessen, GermanyKang, Jun-Suk论文数: 0 引用数: 0 h-index: 0机构: Univ Frankfurt Klinikum, Neurol Klin, Frankfurt, Germany Univ Giessen, Inst Humangenet, D-35392 Giessen, GermanyHilker, Ruediger论文数: 0 引用数: 0 h-index: 0机构: Univ Frankfurt Klinikum, Neurol Klin, Frankfurt, Germany Univ Giessen, Inst Humangenet, D-35392 Giessen, GermanyHackstein, Holger论文数: 0 引用数: 0 h-index: 0机构: Univ Giessen, Inst Transfus Med & Hamotherapie, D-35390 Giessen, Germany Univ Giessen, Inst Humangenet, D-35392 Giessen, GermanyMueller, Ulrich论文数: 0 引用数: 0 h-index: 0机构: Univ Giessen, Inst Humangenet, D-35392 Giessen, Germany Univ Giessen, Inst Humangenet, D-35392 Giessen, GermanyNolte, Dagmar论文数: 0 引用数: 0 h-index: 0机构: Univ Giessen, Inst Humangenet, D-35392 Giessen, Germany Univ Giessen, Inst Humangenet, D-35392 Giessen, Germany
- [5] A Novel Missense Mutation in AFG3L2 Associated with Late Onset and Slow Progression of Spinocerebellar Ataxia Type 28Journal of Molecular Neuroscience, 2014, 52 : 493 - 496Anna Mareike Löbbe论文数: 0 引用数: 0 h-index: 0机构: Justus-Liebig Universität Giessen,Institut für HumangenetikJun-Suk Kang论文数: 0 引用数: 0 h-index: 0机构: Justus-Liebig Universität Giessen,Institut für HumangenetikRüdiger Hilker论文数: 0 引用数: 0 h-index: 0机构: Justus-Liebig Universität Giessen,Institut für HumangenetikHolger Hackstein论文数: 0 引用数: 0 h-index: 0机构: Justus-Liebig Universität Giessen,Institut für HumangenetikUlrich Müller论文数: 0 引用数: 0 h-index: 0机构: Justus-Liebig Universität Giessen,Institut für HumangenetikDagmar Nolte论文数: 0 引用数: 0 h-index: 0机构: Justus-Liebig Universität Giessen,Institut für Humangenetik
- [6] Deletion of AFG3L2 Associated With Spinocerebellar Ataxia Type 28 in the Context of Multiple Genomic AnomaliesAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (12) : 3209 - 3212Myers, Kenneth A.论文数: 0 引用数: 0 h-index: 0机构: Univ Calgary, Dept Pediat, Div Neurol, Alberta Childrens Hosp, Calgary, AB T2N 1N4, Canada Univ Calgary, Dept Pediat, Div Neurol, Alberta Childrens Hosp, Calgary, AB T2N 1N4, CanadaChardon, Jodi Warman论文数: 0 引用数: 0 h-index: 0机构: Univ Ottawa, Childrens Hosp Eastern Ontario, Dept Genet, Ottawa, ON K1H 8L1, Canada Univ Calgary, Dept Pediat, Div Neurol, Alberta Childrens Hosp, Calgary, AB T2N 1N4, CanadaHuang, Lijia论文数: 0 引用数: 0 h-index: 0机构: Univ Ottawa, Childrens Hosp Eastern Ontario, Dept Genet, Ottawa, ON K1H 8L1, Canada Univ Calgary, Dept Pediat, Div Neurol, Alberta Childrens Hosp, Calgary, AB T2N 1N4, CanadaBoycott, Kym M.论文数: 0 引用数: 0 h-index: 0机构: Univ Ottawa, Childrens Hosp Eastern Ontario, Dept Genet, Ottawa, ON K1H 8L1, Canada Univ Calgary, Dept Pediat, Div Neurol, Alberta Childrens Hosp, Calgary, AB T2N 1N4, Canada
- [7] Neurocognitive Characterization of an SCA28 Family Caused by a Novel AFG3L2 Gene MutationCEREBELLUM, 2017, 16 (5-6): : 979 - 985Szpisjak, Laszlo论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, Hungary Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, HungaryNemeth, Viola L.论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, Hungary Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, HungarySzepfalusi, Noemi论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, Hungary Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, HungaryZadori, Denes论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, Hungary Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, HungaryMaroti, Zoltan论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Pediat, Genet Diagnost Lab, Szeged, Hungary Univ Szeged, Pediat Hlth Ctr, Szeged, Hungary Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, HungaryKalmar, Tibor论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Pediat, Genet Diagnost Lab, Szeged, Hungary Univ Szeged, Pediat Hlth Ctr, Szeged, Hungary Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, HungaryVecsei, Laszlo论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, Hungary MTA SZTE Neurosci Res Grp, Szeged, Hungary Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, HungaryKlivenyi, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, Hungary Univ Szeged, Dept Neurol, Semmelweis U 6, H-6725 Szeged, Hungary
- [8] Spinocerebellar Ataxia Type 28-Phenotypic and Molecular Characterization of a Family with Heterozygous and Compound-Heterozygous Mutations in AFG3L2CEREBELLUM, 2019, 18 (04): : 817 - 822Tunc, Sinem论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany Univ Hosp Schleswig Holstein, Dept Neurol, Campus Lubeck, Lubeck, Germany Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, GermanyDulovic-Mahlow, Marija论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, GermanyBaumann, Hauke论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, GermanyBaaske, Magdalena Khira论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany Univ Hosp Schleswig Holstein, Dept Neurol, Campus Lubeck, Lubeck, Germany Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, GermanyJahn, Magdalena论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, GermanyJunker, Johanna论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany Univ Hosp Schleswig Holstein, Dept Neurol, Campus Lubeck, Lubeck, Germany Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, GermanyMuenchau, Alexander论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, GermanyBrueggemann, Norbert论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany Univ Hosp Schleswig Holstein, Dept Neurol, Campus Lubeck, Lubeck, Germany Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, GermanyLohmann, Katja论文数: 0 引用数: 0 h-index: 0机构: Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany Univ Lubeck, Inst Neurogenet, Ratzeburger Allee 160, D-23538 Lubeck, Germany
- [9] Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxiaJOURNAL OF THE NEUROLOGICAL SCIENCES, 2021, 428Chiang, Han-Lin论文数: 0 引用数: 0 h-index: 0机构: Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, Taiwan Natl Yang Ming Chiao Tung Univ, Sch Med, Coll Med, 155,Sec 2,Linong St, Taipei, Taiwan Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, TaiwanFuh, Jong-Ling论文数: 0 引用数: 0 h-index: 0机构: Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, Taiwan Natl Yang Ming Chiao Tung Univ, Sch Med, Coll Med, 155,Sec 2,Linong St, Taipei, Taiwan Natl Yang Ming Chiao Tung Univ, Brain Res Ctr, Sch Med, 155,Sec 2,Linong St, Taipei, Taiwan Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, TaiwanTsai, Yu-Shuen论文数: 0 引用数: 0 h-index: 0机构: Natl Yang Ming Chiao Tung Univ, Ctr Syst & Synthet Biol, 155,Sec 2,Linong St, Taipei 2, Taiwan Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, TaiwanSoong, Bing-Wen论文数: 0 引用数: 0 h-index: 0机构: Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, Taiwan Taipei Med Univ, Shuang Ho Hosp, Dept Neurol, 291 Zhongzheng Rd, New Taipei 23561, Taiwan Taipei Med Univ, Taipei Neurosci Inst, 250 Wu Hsing St, Taipei, Taiwan Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, TaiwanLiao, Yi-Chu论文数: 0 引用数: 0 h-index: 0机构: Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, Taiwan Natl Yang Ming Chiao Tung Univ, Sch Med, Coll Med, 155,Sec 2,Linong St, Taipei, Taiwan Natl Yang Ming Chiao Tung Univ, Brain Res Ctr, Sch Med, 155,Sec 2,Linong St, Taipei, Taiwan Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, TaiwanLee, Yi-Chung论文数: 0 引用数: 0 h-index: 0机构: Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, Taiwan Natl Yang Ming Chiao Tung Univ, Sch Med, Coll Med, 155,Sec 2,Linong St, Taipei, Taiwan Natl Yang Ming Chiao Tung Univ, Brain Res Ctr, Sch Med, 155,Sec 2,Linong St, Taipei, Taiwan Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, 201,Sec 2,Shipai Rd, Taipei, Taiwan
- [10] Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicityNEUROBIOLOGY OF DISEASE, 2019, 124 : 14 - 28Mancini, Cecilia论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyHoxha, Eriola论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Neurosci, Turin, Italy NICO, Orbassano, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyIommarini, Luisa论文数: 0 引用数: 0 h-index: 0机构: Univ Bologna, FABIT, Dept Pharm & Biotechnol, Bologna, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyBrussino, Alessandro论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy论文数: 引用数: h-index:机构:Montarolo, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Neurosci, Turin, Italy NICO, Orbassano, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyCagnoli, Claudia论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyParolisi, Roberta论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Neurosci, Turin, Italy NICO, Orbassano, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyMorosini, Diana Iulia Gondor论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Neurosci, Turin, Italy NICO, Orbassano, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyNicolo, Valentina论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Neurosci, Turin, Italy NICO, Orbassano, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyMaltecca, Francesca论文数: 0 引用数: 0 h-index: 0机构: Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Div Genet & Cell Biol, Milan, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyMuratori, Luisa论文数: 0 引用数: 0 h-index: 0机构: NICO, Orbassano, Italy Univ Torino, Dept Clin & Biol Sci, Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyRonchi, Giulia论文数: 0 引用数: 0 h-index: 0机构: NICO, Orbassano, Italy Univ Torino, Dept Clin & Biol Sci, Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyGeuna, Stefano论文数: 0 引用数: 0 h-index: 0机构: NICO, Orbassano, Italy Univ Torino, Dept Clin & Biol Sci, Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Giorgio, Elisa论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyCavalieri, Simona论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyDi Gregorio, Eleonora论文数: 0 引用数: 0 h-index: 0机构: Citta Salute & Sci Univ Hosp, Med Genet Unit, Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyPozzi, Elisa论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyFerrero, Marta论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyRiberi, Evelise论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Publ Hlth & Pediat, Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyCasari, Giorgio论文数: 0 引用数: 0 h-index: 0机构: Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Div Genet & Cell Biol, Milan, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyAltruda, Fiorella论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Mol Biotechnol & Hlth Sci, Mol Biotechnol Ctr, Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyTurco, Emilia论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Mol Biotechnol & Hlth Sci, Mol Biotechnol Ctr, Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy论文数: 引用数: h-index:机构:Battersby, Brendan J.论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Inst Biotechnol, Helsinki, Finland Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy论文数: 引用数: h-index:机构:Ferrero, Enza论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyBrusco, Alfredo论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy Citta Salute & Sci Univ Hosp, Med Genet Unit, Turin, Italy Univ Bologna, Dept Med & Surg Sci, Med Genet, Bologna, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, ItalyTempia, Filippo论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, Dept Neurosci, Turin, Italy NICO, Orbassano, Italy Univ Bologna, Dept Med & Surg Sci, Med Genet, Bologna, Italy Univ Torino, Dept Med Sci, Via Santena 19, I-10126 Turin, Italy