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- [31] Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephalyHUMAN GENETICS, 2023, 142 (04) : 543 - 552Schnabel, Franziska论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, Germany Univ Leipzig Hosp & Clin, Inst Human Genet, D-04103 Leipzig, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanySchuler, Elisabeth论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Heidelberg, Ctr Paediat & Adolescent Med, Div Paediat Epileptol, Neuenheimer Feld 430, D-69120 Heidelberg, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, Germany论文数: 引用数: h-index:机构:Chaurasia, Ankur论文数: 0 引用数: 0 h-index: 0机构: Manipal Acad Higher Educ, Kasturba Med Coll, Dept Med Genet, Manipal, India Univ Manchester, Fac Biol Med & Hlth, Sch Biol Sci, Div Evolut Infect & Genom, Manchester M13 9PL, Lancs, England Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanySyrbe, Steffen论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Heidelberg, Ctr Paediat & Adolescent Med, Div Paediat Epileptol, Neuenheimer Feld 430, D-69120 Heidelberg, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyAl-Kindi, Adila论文数: 0 引用数: 0 h-index: 0机构: Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Genet, Muscat, Oman Sultan Qaboos Univ Hosp, Genet & Dev Med Clin, Muscat, Oman Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyBhavani, Gandham SriLakshmi论文数: 0 引用数: 0 h-index: 0机构: Manipal Acad Higher Educ, Kasturba Med Coll, Dept Med Genet, Manipal, India Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyShukla, Anju论文数: 0 引用数: 0 h-index: 0机构: Manipal Acad Higher Educ, Kasturba Med Coll, Dept Med Genet, Manipal, India Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyAltmueller, Janine论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne Ctr Genom CCG, Cologne, Germany Univ Cologne, Univ Hosp Cologne, Cologne, Germany Charite Univ Med Berlin, Core Facil Genom, Berlin Inst Hlth, Berlin, Germany Helmholtz Assoc MDC, Max Delbruck Ctr Mol Med, Berlin, Germany Univ Cologne, Fac Med, Ctr Mol Med Cologne CMMC, Cologne, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyNuernberg, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Cologne, Fac Med, Cologne Ctr Genom CCG, Cologne, Germany Univ Cologne, Univ Hosp Cologne, Cologne, Germany Univ Cologne, Fac Med, Ctr Mol Med Cologne CMMC, Cologne, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyBanka, Siddharth论文数: 0 引用数: 0 h-index: 0机构: Univ Manchester, Fac Biol Med & Hlth, Sch Biol Sci, Div Evolut Infect & Genom, Manchester M13 9PL, Lancs, England Manchester Univ NHS Fdn Trust, St Marys Hosp, Manchester Ctr Genom Med, Hlth Innovat Manchester, Manchester M13 9WL, Lancs, England Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyGirisha, Katta M.论文数: 0 引用数: 0 h-index: 0机构: Manipal Acad Higher Educ, Kasturba Med Coll, Dept Med Genet, Manipal, India Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyLi, Yun论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyWollnik, Bernd论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, Germany Univ Gottingen, Cluster Excellence Multiscale Bioimaging Mol Mach, D-37073 Gottingen, Germany DZHK German Ctr Cardiovasc Res, Partner Site Gottingen, Gottingen, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, GermanyYigit, Goekhan论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, Germany DZHK German Ctr Cardiovasc Res, Partner Site Gottingen, Gottingen, Germany Univ Med Ctr Gottingen, Inst Human Genet, Heinrich Duker Weg 12, D-37073 Gottingen, Germany
- [32] Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephalyHuman Genetics, 2023, 142 : 543 - 552Franziska Schnabel论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsElisabeth Schuler论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsAlmundher Al-Maawali论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsAnkur Chaurasia论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsSteffen Syrbe论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsAdila Al-Kindi论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsGandham SriLakshmi Bhavani论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsAnju Shukla论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsJanine Altmüller论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsPeter Nürnberg论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsSiddharth Banka论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsKatta M. Girisha论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsYun Li论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsBernd Wollnik论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human GeneticsGökhan Yigit论文数: 0 引用数: 0 h-index: 0机构: University Medical Center Göttingen,Institute of Human Genetics
- [33] SERKAL syndrome:: An autosomal-recessive disorder caused by a loss-of-function mutation in WNT4AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (01) : 39 - 47Mandel, Hannah论文数: 0 引用数: 0 h-index: 0机构: Meyer Childrens Hosp, Metab Dis Unit, IL-31096 Haifa, Israel Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Fac Med, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelShemer, Revital论文数: 0 引用数: 0 h-index: 0机构: Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Lab Mol Dermatol, IL-31096 Haifa, Israel Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Fac Med, IL-31096 Haifa, Israel Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Ctr Translat Genet, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelBorochowitz, Zvi U.论文数: 0 引用数: 0 h-index: 0机构: Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Fac Med, IL-31096 Haifa, Israel Bnai Zion Med Ctr, Simon Winter Inst Human Genet, IL-31091 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelOkopnik, Marina论文数: 0 引用数: 0 h-index: 0机构: Rambam Hlth Care Campus, Dept Pathol, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelKnopf, Carlos论文数: 0 引用数: 0 h-index: 0机构: Meyer Childrens Hosp, Metab Dis Unit, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelIndelman, Margarita论文数: 0 引用数: 0 h-index: 0机构: Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Lab Mol Dermatol, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelDrugan, Arie论文数: 0 引用数: 0 h-index: 0机构: Rambam Hlth Care Campus, Dept Obstet & Gynecol, IL-31096 Haifa, Israel Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Fac Med, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelTiosano, Dov论文数: 0 引用数: 0 h-index: 0机构: Rambam Hlth Care Campus, Dept Pediat Endocrinol, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelGershoni-Baruch, Ruth论文数: 0 引用数: 0 h-index: 0机构: Rambam Hlth Care Campus, Inst Genet, IL-31096 Haifa, Israel Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Fac Med, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelChoder, Mordechai论文数: 0 引用数: 0 h-index: 0机构: Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Fac Med, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, IsraelSprecher, Eli论文数: 0 引用数: 0 h-index: 0机构: Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Lab Mol Dermatol, IL-31096 Haifa, Israel Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Fac Med, IL-31096 Haifa, Israel Technion Israel Inst Technol, Rappaport Family Inst Res Med Sci, Ctr Translat Genet, IL-31096 Haifa, Israel Rambam Hlth Care Campus, Dept Dermatol, IL-31096 Haifa, Israel
- [34] Loss-of-function mutations in Carboxypeptidase D cause a new syndrome with lymphedema and sensorineural hearing lossMECHANISMS OF DEVELOPMENT, 2017, 145 : S32 - S32Laupheimer, Simone论文数: 0 引用数: 0 h-index: 0机构: IA STAR, Singapore, Singapore IA STAR, Singapore, SingaporeSzenker, Emmanuelle论文数: 0 引用数: 0 h-index: 0机构: IA STAR, Singapore, Singapore IA STAR, Singapore, SingaporeAltunoglu, Umut论文数: 0 引用数: 0 h-index: 0机构: Koc Univ, Sch Med, Istanbul, Turkey IA STAR, Singapore, SingaporeKayserili, Hulya论文数: 0 引用数: 0 h-index: 0机构: Koc Univ, Sch Med, Istanbul, Turkey IA STAR, Singapore, SingaporeReversade, Bruno论文数: 0 引用数: 0 h-index: 0机构: IA STAR, Singapore, Singapore Koc Univ, Sch Med, Istanbul, Turkey IA STAR, Singapore, Singapore
- [35] Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humansJournal of Human Genetics, 2019, 64 : 257 - 260Alex Marcel Moreira Dias论文数: 0 引用数: 0 h-index: 0机构: Universidade de São Paulo,Centro de Pesquisas sobre o Genoma Humano e CélulasKarina Lezirovitz论文数: 0 引用数: 0 h-index: 0机构: Universidade de São Paulo,Centro de Pesquisas sobre o Genoma Humano e CélulasFernanda Stávale Nicastro论文数: 0 引用数: 0 h-index: 0机构: Universidade de São Paulo,Centro de Pesquisas sobre o Genoma Humano e CélulasBeatriz C. A. Mendes论文数: 0 引用数: 0 h-index: 0机构: Universidade de São Paulo,Centro de Pesquisas sobre o Genoma Humano e CélulasRegina Célia Mingroni-Netto论文数: 0 引用数: 0 h-index: 0机构: Universidade de São Paulo,Centro de Pesquisas sobre o Genoma Humano e Células
- [36] Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humansJOURNAL OF HUMAN GENETICS, 2019, 64 (03) : 257 - 260Moreira Dias, Alex Marcel论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Dept Genet & Biol Evolut, Inst Biociencias, Ctr Pesquisas Genoma Humano & Celulas Tronco, Sao Paulo, Brazil Univ Sao Paulo, Dept Genet & Biol Evolut, Inst Biociencias, Ctr Pesquisas Genoma Humano & Celulas Tronco, Sao Paulo, BrazilLezirovitz, Karina论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Dept Genet & Biol Evolut, Inst Biociencias, Ctr Pesquisas Genoma Humano & Celulas Tronco, Sao Paulo, Brazil Univ Sao Paulo, Fac Med, Hosp Clin, Lab Otorrinolaringol LIM32, Sao Paulo, Brazil Univ Sao Paulo, Dept Genet & Biol Evolut, Inst Biociencias, Ctr Pesquisas Genoma Humano & Celulas Tronco, Sao Paulo, BrazilNicastro, Fernanda Stavale论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catolica Sao Paulo, Divisdo Educ & Reabilitacao Disturbios Comun, Sao Paulo, Brazil Univ Sao Paulo, Dept Genet & Biol Evolut, Inst Biociencias, Ctr Pesquisas Genoma Humano & Celulas Tronco, Sao Paulo, BrazilMendes, Beatriz C. A.论文数: 0 引用数: 0 h-index: 0机构: Pontificia Univ Catolica Sao Paulo, Divisdo Educ & Reabilitacao Disturbios Comun, Sao Paulo, Brazil Univ Sao Paulo, Dept Genet & Biol Evolut, Inst Biociencias, Ctr Pesquisas Genoma Humano & Celulas Tronco, Sao Paulo, BrazilMingroni-Netto, Regina Celia论文数: 0 引用数: 0 h-index: 0机构: Univ Sao Paulo, Dept Genet & Biol Evolut, Inst Biociencias, Ctr Pesquisas Genoma Humano & Celulas Tronco, Sao Paulo, Brazil Univ Sao Paulo, Dept Genet & Biol Evolut, Inst Biociencias, Ctr Pesquisas Genoma Humano & Celulas Tronco, Sao Paulo, Brazil
- [37] High-Throughput Sequencing Reveals the Loss-of-Function Mutations in GALT Cause Recessive Classical GalactosemiaFRONTIERS IN PEDIATRICS, 2020, 8Li, Lulu论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R China Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R ChinaMa, Li论文数: 0 引用数: 0 h-index: 0机构: Hebei Prov Childrens Hosp, Dept Neonatol, Shijiazhuang, Hebei, Peoples R China Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R ChinaSun, Min论文数: 0 引用数: 0 h-index: 0机构: Hebei Prov Childrens Hosp, Dept Neonatol, Shijiazhuang, Hebei, Peoples R China Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R ChinaJiao, Jiancheng论文数: 0 引用数: 0 h-index: 0机构: Hebei Prov Childrens Hosp, Dept Neonatol, Shijiazhuang, Hebei, Peoples R China Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R ChinaZhang, Yudong论文数: 0 引用数: 0 h-index: 0机构: Hebei Prov Childrens Hosp, Dept Neonatol, Shijiazhuang, Hebei, Peoples R China Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R ChinaTang, Yue论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R China Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R ChinaYang, Nan论文数: 0 引用数: 0 h-index: 0机构: Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R China Capital Med Univ, Dept Newborn Screening Ctr, Beijing Obstet & Gynecol Hosp, Beijing Maternal & Child Hlth Care Hosp, Beijing, Peoples R China论文数: 引用数: h-index:机构:
- [38] Loss-of-function variants in POPDC2 cause a novel autosomal recessive syndrome with sinus node disease and AV conduction defects in combination with hypertrophic cardiomyopathyEUROPEAN JOURNAL OF HUMAN GENETICS, 2024, 32 : 58 - 59Nicastro, Michele论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsVermeer, Alexa论文数: 0 引用数: 0 h-index: 0机构: Amsterdam Dept Human Genet, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsPostema, Pieter论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsBowling, Forrest论文数: 0 引用数: 0 h-index: 0机构: SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY USA Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlands论文数: 引用数: h-index:机构:Postma, Alex论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Med Biol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsLodder, Elisabeth论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlandsvan Duijvenboden, Karel论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Med Biol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsZwart, Rob论文数: 0 引用数: 0 h-index: 0机构: Amsterdam Dept Human Genet, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsBeekman, Leander论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlandsvan der Zwaag, Paul论文数: 0 引用数: 0 h-index: 0机构: Univ Groningen, Dept Genet, Univ Med Ctr Groningen, Groningen, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsAguib, Yasmine论文数: 0 引用数: 0 h-index: 0机构: Aswan Heart Ctr Magdi Yacoub Fdn, Aswan, Egypt Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsAllouba, Mona论文数: 0 引用数: 0 h-index: 0机构: Imperial Coll London, NHLI, London, England Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsSantome, Luis论文数: 0 引用数: 0 h-index: 0机构: Hlth Code, Coruna, Spain Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsDeuna, David论文数: 0 引用数: 0 h-index: 0机构: Hlth Code, Coruna, Spain Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsMonserrat, Lorenzo论文数: 0 引用数: 0 h-index: 0机构: Dilemma Solut SL, Dept Med, Corona, Spain Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsFortunato, Francesco论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dino Ferrari Ctr, Dept Pathophysiol & Transplantat, Milan, Italy Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsComi, Giacomo论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dino Ferrari Ctr, Dept Pathophysiol & Transplantat, Milan, Italy Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsRonchi, Dario论文数: 0 引用数: 0 h-index: 0机构: Univ Milan, Dino Ferrari Ctr, Dept Pathophysiol & Transplantat, Milan, Italy Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlandsvan Tintelen, Peter论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Utrecht, Dept Clin Genet, Utrecht, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsAirola, Michael论文数: 0 引用数: 0 h-index: 0机构: SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY USA Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsChristiaans, Imke论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsWilde, Arthur论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsWilders, Ronald论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Med Biol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsClur, Sally-ann论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Emma Childrens Hosp, Dept Pediat Cardiol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsVerkerk, Arie论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Med Biol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsBezzina, Connie R.论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, NetherlandsLahrouchi, Najim论文数: 0 引用数: 0 h-index: 0机构: Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlands Amsterdam UMC, Dept Clin & Expt Cardiol, Amsterdam, Netherlands
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