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- [1] Phenotypic variability of patients with an identical SHOC2 variantEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 1445 - 1445Buurman, Reena论文数: 0 引用数: 0 h-index: 0机构: Hannover Med Sch, Inst Human Genet, Hannover, Germany Hannover Med Sch, Inst Human Genet, Hannover, GermanyThiel, Karsten论文数: 0 引用数: 0 h-index: 0机构: St Clemens Hosp Geldern, Clin Children & Adolescent Care, Geldern, Germany Hannover Med Sch, Inst Human Genet, Hannover, GermanyBaumann, Ulrich论文数: 0 引用数: 0 h-index: 0机构: Hannover Med Sch, Pediat Pneumol Allergol & Neonatol, Hannover, Germany Hannover Med Sch, Inst Human Genet, Hannover, GermanyDi Donato, Nataliya论文数: 0 引用数: 0 h-index: 0机构: Hannover Med Sch, Inst Human Genet, Hannover, Germany Hannover Med Sch, Inst Human Genet, Hannover, Germanyvon Hardenberg, Sandra论文数: 0 引用数: 0 h-index: 0机构: Hannover Med Sch, Inst Human Genet, Hannover, Germany Hannover Med Sch, Inst Human Genet, Hannover, GermanyAuber, Bernd论文数: 0 引用数: 0 h-index: 0机构: Hannover Med Sch, Inst Human Genet, Hannover, Germany Hannover Med Sch, Inst Human Genet, Hannover, Germany
- [2] Recurrent Erythema Nodosum in a Child with a SHOC2 Gene MutationYONAGO ACTA MEDICA, 2019, 62 (01) : 159 - 162论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Sugita, Kazunari论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ, Sch Med, Dept Med Sensory & Motor Organs, Div Dermatol,Fac Med, Yonago, Tottori 6838504, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanNosaka, Kanae论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ, Sch Med, Dept Pathol, Div Organ Pathol,Fac Med, Yonago, Tottori 6838504, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanOhno, Koyo论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanHiraoka, Yumie论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ Hosp, Dept Clin Genet, Yonago, Tottori 6838504, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanKasagi, Noriko论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ Hosp, Dept Clin Genet, Yonago, Tottori 6838504, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanEbiki, Mitsutaka论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ, Grad Sch Med Sci, Dev Innovat Future Med Treatment, Yonago, Tottori 6838504, Japan KUSUNOKI SCALE Inc, Yonago, Tottori 6830832, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanNarai, Satoshi论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ, Fac Med, Div Pediat & Perinatol, Dept Multidisciplinary Internal Med,Sch Med, Yonago, Tottori 6838504, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanKawashima, Yuki论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ, Fac Med, Div Pediat & Perinatol, Dept Multidisciplinary Internal Med,Sch Med, Yonago, Tottori 6838504, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanTakano, Shuichi论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ, Fac Med, Div Surg Oncol, Dept Surg,Sch Med, Yonago, Tottori 6838504, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanKai, Masachika论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ, Div Tech Dept, Yonago, Tottori 6838503, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, Japan论文数: 引用数: h-index:机构:Yamamoto, Osamu论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ, Sch Med, Dept Med Sensory & Motor Organs, Div Dermatol,Fac Med, Yonago, Tottori 6838504, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, JapanNanba, Eiji论文数: 0 引用数: 0 h-index: 0机构: Tottori Univ Hosp, Dept Clin Genet, Yonago, Tottori 6838504, Japan Tottori Univ, Res Strategy Div, Org Res Initiat & Promot, Yonago, Tottori 6838503, Japan Tottori Univ, Fac Med, Div Child Neurol, Dept Brain & Neurosci,Sch Med, Yonago, Tottori 6838504, Japan论文数: 引用数: h-index:机构:
- [3] Phenotypic Variability Associated With the Invariant SHOC2 c.4A>G (p.Ser2Gly) Missense MutationAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (12) : 3120 - 3125Baldassarre, Giuseppina论文数: 0 引用数: 0 h-index: 0机构: Univ Turin, Dept Paediat, I-10126 Turin, Italy Univ Turin, Dept Paediat, I-10126 Turin, Italy论文数: 引用数: h-index:机构:Banaudi, Elena论文数: 0 引用数: 0 h-index: 0机构: Regina Margherita Childrens Hosp, Dept Cardiol, Turin, Italy Univ Turin, Dept Paediat, I-10126 Turin, ItalyRossi, Cesare论文数: 0 引用数: 0 h-index: 0机构: St Orsola Marcello Malpighi Hosp, Dept Med Genet, Bologna, Italy Univ Turin, Dept Paediat, I-10126 Turin, ItalyTartaglia, Marco论文数: 0 引用数: 0 h-index: 0机构: Ist Super Sanita, Dept Haematol Oncol & Mol Med, I-00161 Rome, Italy Univ Turin, Dept Paediat, I-10126 Turin, ItalySilengo, Margherita论文数: 0 引用数: 0 h-index: 0机构: Univ Turin, Dept Paediat, I-10126 Turin, Italy Univ Turin, Dept Paediat, I-10126 Turin, Italy论文数: 引用数: h-index:机构:
- [4] Clinical Heterogeneity in two patients with Noonan-like Syndrome associated with the same SHOC2 mutationItalian Journal of Pediatrics, 38Donatella Capalbo论文数: 0 引用数: 0 h-index: 0机构: “Federico II” University of Naples,Department of PediatricsMaria Giuseppa Scala论文数: 0 引用数: 0 h-index: 0机构: “Federico II” University of Naples,Department of PediatricsDaniela Melis论文数: 0 引用数: 0 h-index: 0机构: “Federico II” University of Naples,Department of PediatricsGiorgia Minopoli论文数: 0 引用数: 0 h-index: 0机构: “Federico II” University of Naples,Department of PediatricsNicola Improda论文数: 0 引用数: 0 h-index: 0机构: “Federico II” University of Naples,Department of PediatricsLoredana Palamaro论文数: 0 引用数: 0 h-index: 0机构: “Federico II” University of Naples,Department of PediatricsClaudio Pignata论文数: 0 引用数: 0 h-index: 0机构: “Federico II” University of Naples,Department of PediatricsMariacarolina Salerno论文数: 0 引用数: 0 h-index: 0机构: “Federico II” University of Naples,Department of Pediatrics
- [5] Protein-Losing Enteropathy Associated With SHOC2 Gene Mutation in Noonan-Like SyndromeAMERICAN JOURNAL OF GASTROENTEROLOGY, 2022, 117 (10): : S2182 - S2183Ancha, Anupama论文数: 0 引用数: 0 h-index: 0机构: Baylor Scott & White Med Ctr, Temple, TX USA Baylor Scott & White Med Ctr, Temple, TX USABejcek, Alexis论文数: 0 引用数: 0 h-index: 0机构: Baylor Scott & White Med Ctr, Temple, TX USA Baylor Scott & White Med Ctr, Temple, TX USAJohnson, Christopher论文数: 0 引用数: 0 h-index: 0机构: Baylor Scott & White Med Ctr, Temple, TX USA Baylor Scott & White Med Ctr, Temple, TX USA
- [6] Clinical Heterogeneity in two patients with Noonan-like Syndrome associated with the same SHOC2 mutationITALIAN JOURNAL OF PEDIATRICS, 2013, 38Capalbo, Donatella论文数: 0 引用数: 0 h-index: 0机构: Univ Naples Federico II, Dept Pediat, Naples, Italy Univ Naples Federico II, Dept Pediat, Naples, ItalyScala, Maria Giuseppa论文数: 0 引用数: 0 h-index: 0机构: Univ Naples Federico II, Dept Pediat, Naples, Italy Univ Naples Federico II, Dept Pediat, Naples, Italy论文数: 引用数: h-index:机构:Minopoli, Giorgia论文数: 0 引用数: 0 h-index: 0机构: Univ Naples Federico II, Dept Pediat, Naples, Italy Univ Naples Federico II, Dept Pediat, Naples, ItalyImproda, Nicola论文数: 0 引用数: 0 h-index: 0机构: Univ Naples Federico II, Dept Pediat, Naples, Italy Univ Naples Federico II, Dept Pediat, Naples, Italy论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:
- [7] A Novel SHOC2 Variant in RasopathyHUMAN MUTATION, 2014, 35 (11) : 1290 - 1294Hannig, Vickie论文数: 0 引用数: 0 h-index: 0机构: Vanderbilt Univ, Div Med Genet & Genom Med, Nashville, TN 37235 USA Vanderbilt Univ, Div Med Genet & Genom Med, Nashville, TN 37235 USAJeoung, Myoungkun论文数: 0 引用数: 0 h-index: 0机构: Univ Kentucky, Dept Mol & Cellular Biochem, Lexington, KY USA Vanderbilt Univ, Div Med Genet & Genom Med, Nashville, TN 37235 USAJang, Eun Ryoung论文数: 0 引用数: 0 h-index: 0机构: Univ Kentucky, Dept Mol & Cellular Biochem, Lexington, KY USA Vanderbilt Univ, Div Med Genet & Genom Med, Nashville, TN 37235 USAPhillips, John A., III论文数: 0 引用数: 0 h-index: 0机构: Vanderbilt Univ, Div Med Genet & Genom Med, Nashville, TN 37235 USA Vanderbilt Univ, Div Med Genet & Genom Med, Nashville, TN 37235 USAGalperin, Emilia论文数: 0 引用数: 0 h-index: 0机构: Univ Kentucky, Dept Mol & Cellular Biochem, Lexington, KY USA Vanderbilt Univ, Div Med Genet & Genom Med, Nashville, TN 37235 USA
- [8] Expanding the molecular spectrum of pathogenic SHOC2 variants underlying Mazzanti syndromeHUMAN MOLECULAR GENETICS, 2022, 31 (16) : 2766 - 2778Motta, Marialetizia论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalySolman, Maja论文数: 0 引用数: 0 h-index: 0机构: Hubrecht Inst KNAW, NL-3584 Utrecht, Netherlands Univ Med Ctr Utrecht, NL-3584 Utrecht, Netherlands IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyBonnard, Adeline A.论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, AP HP, Dept Genet, F-75019 Paris, France Univ Paris, INSERM UMR 1131, Inst Rech St Louis, F-75010 Paris, France IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyKuechler, Alma论文数: 0 引用数: 0 h-index: 0机构: Univ Duisburg Essen, Univ Klinikum Essen, Inst Humangenet, D-45147 Essen, Germany IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyPantaleoni, Francesca论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyPriolo, Manuela论文数: 0 引用数: 0 h-index: 0机构: Grandeosped Metropolitano Bianchi Melacrino Morel, UOSD Genet Med, I-89124 Reggio Di Calabria, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyChandramouli, Balasubramanian论文数: 0 引用数: 0 h-index: 0机构: CINECA, Super Comp Applicat & Innovat, I-40033 Bologna, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyCoppola, Simona论文数: 0 引用数: 0 h-index: 0机构: Ist Super Sanita, Natl Ctr Rare Dis, I-00161 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyPizzi, Simone论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyZara, Erika论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, Italy Sapienza Univ Rome, Dept Biol & Biotechnol Charles Darwin, I-00185 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyFerilli, Marco论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyKayserili, Hulya论文数: 0 引用数: 0 h-index: 0机构: Koc Univ, Genet Dis Evaluat Ctr, Med Genet Dept, Sch Med, TR-34010 Istanbul, Turkey IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyOnesimo, Roberta论文数: 0 引用数: 0 h-index: 0机构: Fdn Policlin Univ A Gemelli, Ctr Rare Dis & Birth Defects, Dept Woman & Child Hlth & Publ Hlth, IRCCS, I-00168 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyLeoni, Chiara论文数: 0 引用数: 0 h-index: 0机构: Fdn Policlin Univ A Gemelli, Ctr Rare Dis & Birth Defects, Dept Woman & Child Hlth & Publ Hlth, IRCCS, I-00168 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyBrinkmann, Julia论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Magdeburg, Inst Human Genet, D-39120 Magdeburg, Germany IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyVial, Yoann论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, AP HP, Dept Genet, F-75019 Paris, France Univ Paris, INSERM UMR 1131, Inst Rech St Louis, F-75010 Paris, France IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyKamphausen, Susanne B.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Magdeburg, Inst Human Genet, D-39120 Magdeburg, Germany IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyThomas-Teinturier, Cecile论文数: 0 引用数: 0 h-index: 0机构: Univ Paris Saclay, Hop Bicetre, AP HP, Dept Pediat Endocrinol, F-94270 Le Kremlin Bicetre, France CESP, Canc & Radiat Team, INSERM UMR 1018, F-94800 Villejuif, France IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyGuimier, Anne论文数: 0 引用数: 0 h-index: 0机构: Hop Necker Enfants Malad, AP HP, Serv Med Genom Malad Rares, CRMR Anomalies Dev, F-75015 Paris, France IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyCordeddu, Viviana论文数: 0 引用数: 0 h-index: 0机构: Ist Super Sanita, Dept Oncol & Mol Med, I-00161 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyMazzanti, Laura论文数: 0 引用数: 0 h-index: 0机构: Alma Mater Studiorum Univ Bologna, I-40125 Bologna, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyZampino, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Fdn Policlin Univ A Gemelli, Ctr Rare Dis & Birth Defects, Dept Woman & Child Hlth & Publ Hlth, IRCCS, I-00168 Rome, Italy Univ Cattolica Sacro Cuore, Dept Woman & Child Hlth & Publ Hlth, I-00168 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyChillemi, Giovanni论文数: 0 引用数: 0 h-index: 0机构: Univ Tuscia, Dept Innovat Biol Agrofood & Forest Syst, I-01100 Viterbo, Italy Ctr Nazl Ric, Ist Biomembrane Bioenerget & Biotecnol Molecolari, I-70126 Bari, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyZenker, Martin论文数: 0 引用数: 0 h-index: 0机构: Univ Duisburg Essen, Univ Klinikum Essen, Inst Humangenet, D-45147 Essen, Germany IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyCave, Helene论文数: 0 引用数: 0 h-index: 0机构: Hop Robert Debre, AP HP, Dept Genet, F-75019 Paris, France Univ Paris, INSERM UMR 1131, Inst Rech St Louis, F-75010 Paris, France IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyHertog, Jeroen论文数: 0 引用数: 0 h-index: 0机构: Hubrecht Inst KNAW, NL-3584 Utrecht, Netherlands Univ Med Ctr Utrecht, NL-3584 Utrecht, Netherlands IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, ItalyTartaglia, Marco论文数: 0 引用数: 0 h-index: 0机构: IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, Italy IRCCS, Genet & Rare Dis Res Div, Osped Pediat Bambino Gesu, I-00146 Rome, Italy
- [9] The Role of Shoc2 in Regulating Cell MotilityFASEB JOURNAL, 2013, 27Jang, Hye In论文数: 0 引用数: 0 h-index: 0机构: Univ Kentucky, Lexington, KY USA Univ Kentucky, Lexington, KY USAJeoung, Myoungjun论文数: 0 引用数: 0 h-index: 0机构: Univ Kentucky, Lexington, KY USA Univ Kentucky, Lexington, KY USA论文数: 引用数: h-index:机构:
- [10] Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignanciesJournal of Human Genetics, 2010, 55 : 801 - 809Shoko Komatsuzaki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsYoko Aoki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsTetsuya Niihori论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsNobuhiko Okamoto论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsRaoul C M Hennekam论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsSaskia Hopman论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsHirofumi Ohashi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsSeiji Mizuno论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsYoriko Watanabe论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsHotaka Kamasaki论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsIkuko Kondo论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsNobuko Moriyama论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsKenji Kurosawa论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsHiroshi Kawame论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsRyuhei Okuyama论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsMasue Imaizumi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsTakeshi Rikiishi论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsShigeru Tsuchiya论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsShigeo Kure论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical GeneticsYoichi Matsubara论文数: 0 引用数: 0 h-index: 0机构: Tohoku University School of Medicine,Department of Medical Genetics