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- [1] CLINICAL SPECTRUM OF OHTAHARA SYNDROME CAUSED BY STXBP1 MUTATIONEPILEPSIA, 2009, 50 : 16 - 17Kato, M.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Sch Med, Yamagata 990, Japan Yamagata Univ, Sch Med, Yamagata 990, Japan论文数: 引用数: h-index:机构:Mizuguchi, T.论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Yokohama, Kanagawa, Japan Yamagata Univ, Sch Med, Yamagata 990, JapanOsaka, H.论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Clin Res Inst, Kanagawa, Japan Yamagata Univ, Sch Med, Yamagata 990, JapanTohyama, J.论文数: 0 引用数: 0 h-index: 0机构: Nishi Niigata Chuo Natl Hosp, Epilepsy Ctr, Niigata, Japan Yamagata Univ, Sch Med, Yamagata 990, JapanUruno, K.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Natl Hosp, Epilepsy Ctr, Yamagata, Japan Yamagata Univ, Sch Med, Yamagata 990, JapanKumada, S.论文数: 0 引用数: 0 h-index: 0机构: Tokyo Metropolitan Neurol Hosp, Tokyo, Japan Yamagata Univ, Sch Med, Yamagata 990, JapanHamada, K.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Sch Med, Yamagata 990, JapanNishimura, A.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Sch Med, Yamagata 990, JapanHirai, S.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Sch Med, Yamagata 990, JapanKumada, T.论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Hamamatsu, Shizuoka, Japan Yamagata Univ, Sch Med, Yamagata 990, JapanFukuda, A.论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Hamamatsu, Shizuoka, Japan Yamagata Univ, Sch Med, Yamagata 990, JapanOgata, K.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Sch Med, Yamagata 990, JapanHayasaka, K.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Sch Med, Yamagata 990, Japan Yamagata Univ, Sch Med, Yamagata 990, JapanMatsumoto, N.论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Yokohama, Kanagawa, Japan Yamagata Univ, Sch Med, Yamagata 990, Japan
- [2] STXBP1 encephalopathies: Clinical spectrum, disease mechanisms, and therapeutic strategiesJOURNAL OF NEUROCHEMISTRY, 2021, 157 (02) : 165 - 178Abramov, Debra论文数: 0 引用数: 0 h-index: 0机构: Weill Cornell Med, Appel Inst Alzheimers Dis Res, Brain & Mind Res Inst, 413 East 69th St, New York, NY 10021 USA Weill Cornell Med, Appel Inst Alzheimers Dis Res, Brain & Mind Res Inst, 413 East 69th St, New York, NY 10021 USAGuiberson, Noah Guy Lewis论文数: 0 引用数: 0 h-index: 0机构: Weill Cornell Med, Appel Inst Alzheimers Dis Res, Brain & Mind Res Inst, 413 East 69th St, New York, NY 10021 USA Weill Cornell Med, Appel Inst Alzheimers Dis Res, Brain & Mind Res Inst, 413 East 69th St, New York, NY 10021 USABurre, Jacqueline论文数: 0 引用数: 0 h-index: 0机构: Weill Cornell Med, Appel Inst Alzheimers Dis Res, Brain & Mind Res Inst, 413 East 69th St, New York, NY 10021 USA Weill Cornell Med, Appel Inst Alzheimers Dis Res, Brain & Mind Res Inst, 413 East 69th St, New York, NY 10021 USA
- [3] STXBP1: CLINICAL AND GENETIC DESCRIPTION OF 39 NEW PATIENTS WITH AN STXBP1 MUTATION AND REVIEW OF LITERATUREEPILEPSIA, 2015, 56 : 220 - 220论文数: 引用数: h-index:机构:Nikanorova, M.论文数: 0 引用数: 0 h-index: 0机构: Danish Epilepsy Ctr, Dianalund, Denmark Univ Childrens Hosp, Inselspital, Div Human Genet, Bern, Switzerland 19Univ Southern Denmark, Inst Reg Hlth Serv, Odense, Denmark VIB DMG, Neurogenet Grp, Antwerp, BelgiumWillemsen, M.论文数: 0 引用数: 0 h-index: 0机构: Radboud Univ Nijmegen Med Ctr, Dept Human Genet, Nijmegen, Netherlands VIB DMG, Neurogenet Grp, Antwerp, BelgiumFjaer, R.论文数: 0 引用数: 0 h-index: 0机构: Oslo Univ Hosp, Med Genet, Oslo, Norway VIB DMG, Neurogenet Grp, Antwerp, BelgiumRamsey, K.论文数: 0 引用数: 0 h-index: 0机构: Translat Genom Res Inst, Neurogen Div, Phoenix, AZ USA VIB DMG, Neurogenet Grp, Antwerp, BelgiumViri, M.论文数: 0 引用数: 0 h-index: 0机构: Fatebenefratelli & Oftalm Hosp, Pediat Neurol Unit, Milan, Italy Epilepsy Ctr, Dept Neurosci, Milan, Italy VIB DMG, Neurogenet Grp, Antwerp, BelgiumSterbova, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Motol, Child Neurol Dept, Prague, Czech Republic VIB DMG, Neurogenet Grp, Antwerp, BelgiumWolf, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp, Dept Pediat Neurol, Tubingen, Germany VIB DMG, Neurogenet Grp, Antwerp, BelgiumVerhelst, H.论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Dept Pediat, Div Pediat Neurol & Metab, Ghent, Belgium VIB DMG, Neurogenet Grp, Antwerp, BelgiumBenkel, I.论文数: 0 引用数: 0 h-index: 0机构: Sana Krankenhaus Gerresheim, Dept Neuropediat, Dusseldorf, Germany VIB DMG, Neurogenet Grp, Antwerp, BelgiumFannemel, M.论文数: 0 引用数: 0 h-index: 0机构: Oslo Univ Hosp, Dept Med Genet, Oslo, Norway VIB DMG, Neurogenet Grp, Antwerp, BelgiumMuehle, H.论文数: 0 引用数: 0 h-index: 0机构: Univ Kiel, Dept Neuropediat, Univ Med Ctr Schleswig Holstein, Kiel, Germany VIB DMG, Neurogenet Grp, Antwerp, BelgiumCasara, G.论文数: 0 引用数: 0 h-index: 0机构: Cent Hosp Bolzano, Neurol Unit & Labs, Bolzano, Italy VIB DMG, Neurogenet Grp, Antwerp, BelgiumVan Coster, R.论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Dept Pediat, Div Pediat Neurol & Metab, Ghent, Belgium VIB DMG, Neurogenet Grp, Antwerp, BelgiumAngriman, M.论文数: 0 引用数: 0 h-index: 0机构: Cent Hosp Bolzano, Neurol Unit & Labs, Bolzano, Italy VIB DMG, Neurogenet Grp, Antwerp, BelgiumLederer, D.论文数: 0 引用数: 0 h-index: 0机构: Inst Pathol & Genet, Gosseliers, Belgium VIB DMG, Neurogenet Grp, Antwerp, BelgiumDe Jonghe, P.论文数: 0 引用数: 0 h-index: 0机构: VIB DMG, Neurogenet Grp, Antwerp, Belgium Univ Hosp Leipzig, Inst Human Genet, Leipzig, Germany VIB DMG, Neurogenet Grp, Antwerp, BelgiumStriano, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Genoa, Dept Neurosci, Inst G Gaslini, Pediat Neurol & Neuromuscular Dis Unit, Genoa, Italy VIB DMG, Neurogenet Grp, Antwerp, BelgiumLemke, J.论文数: 0 引用数: 0 h-index: 0机构: VIB DMG, Neurogenet Grp, Antwerp, BelgiumMoller, R. S.论文数: 0 引用数: 0 h-index: 0机构: Danish Epilepsy Ctr, Dianalund, Denmark Univ Childrens Hosp, Inselspital, Div Human Genet, Bern, Switzerland 19Univ Southern Denmark, Inst Reg Hlth Serv, Odense, Denmark VIB DMG, Neurogenet Grp, Antwerp, BelgiumWeckhuysen, S.论文数: 0 引用数: 0 h-index: 0机构: VIB DMG, Neurogenet Grp, Antwerp, Belgium Hop La Pitie Salpetriere, Inst Cerveau & Moelle Epiniere, Paris, France VIB DMG, Neurogenet Grp, Antwerp, Belgium
- [4] Genotype and phenotype spectrum of 10 children with STXBP1 gene-related encephalopathy and epilepsyFRONTIERS IN PEDIATRICS, 2022, 10Dong, Meng论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R ChinaZhang, Tianyu论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R ChinaHu, Ruimei论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R ChinaLi, Meng论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R ChinaWang, Guan论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R ChinaLiu, Xinjie论文数: 0 引用数: 0 h-index: 0机构: Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R China Shandong Univ, Qilu Hosp, Dept Pediat, Jinan, Peoples R China
- [5] Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutationsNEUROLOGY, 2010, 75 (13) : 1159 - 1165Deprez, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Res Grp, Antwerp, Belgium Inst Born Bunge, Antwerp, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumWeckhuysen, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Res Grp, Antwerp, Belgium Inst Born Bunge, Antwerp, Belgium Epilepsy Ctr Kempenhaeghe, Oosterhout, Netherlands Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumHolmgren, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Res Grp, Antwerp, Belgium Inst Born Bunge, Antwerp, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumSuls, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Res Grp, Antwerp, Belgium Inst Born Bunge, Antwerp, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumVan Dyck, T.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Res Grp, Antwerp, Belgium Inst Born Bunge, Antwerp, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumGoossens, D.论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Appl Mol Genom Grp, Antwerp, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumDel-Favero, J.论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Appl Mol Genom Grp, Antwerp, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumJansen, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Res Grp, Antwerp, Belgium Inst Born Bunge, Antwerp, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumVerhaert, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumLagae, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Gasthuisberg, Dept Pediat Neurol, B-3000 Louvain, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumJordanova, A.论文数: 0 引用数: 0 h-index: 0机构: UZ Brussel, Pediat Neurol Unit, Dept Pediat, Brussels, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumVan Coster, R.论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Dept Pediat, B-9000 Ghent, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumYendle, S.论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Div Pediat Neurol, Dept Med, B-9000 Ghent, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumBerkovic, S. F.论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Div Pediat Neurol, Dept Med, B-9000 Ghent, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumScheffer, I.论文数: 0 引用数: 0 h-index: 0机构: Ghent Univ Hosp, Div Pediat Neurol, Dept Med, B-9000 Ghent, Belgium Univ Melbourne, Epilepsy Res Ctr, Austin Hlth, Melbourne, Vic, Australia Univ Melbourne, Dept Pediat, Royal Childrens Hosp, Melbourne, Vic, Australia Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumCeulemans, B.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Res Grp, Antwerp, BelgiumDe Jonghe, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Antwerp, Neurogenet Res Grp, Antwerp, Belgium Inst Born Bunge, Antwerp, Belgium Univ Antwerp Hosp, Dept Neurol, Antwerp, Belgium Univ Antwerp, Neurogenet Res Grp, Antwerp, Belgium
- [6] Phenotypic spectrum of STXBP1 gene mutations - Case seriesEPILEPSIA, 2024, 65 : 307 - 308Radova, S.论文数: 0 引用数: 0 h-index: 0机构: Comenius Univ, Fac Med, Bratislava, Slovakia Natl Inst Childrens Dis, Dept Paediat Neurol, Bratislava, Slovakia Comenius Univ, Fac Med, Bratislava, SlovakiaGrunnerova, L.论文数: 0 引用数: 0 h-index: 0机构: Comenius Univ, Inst Med Chem Biochem & Clin Biochem, Dept Clin Genet, Bratislava, Slovakia Comenius Univ, Fac Med, Bratislava, SlovakiaRivera, G. A. Ramos论文数: 0 引用数: 0 h-index: 0机构: Martin Univ Hosp, Dept Paediat, Martin, Slovakia Comenius Univ, Fac Med, Bratislava, SlovakiaKolnikova, M.论文数: 0 引用数: 0 h-index: 0机构: Comenius Univ, Fac Med, Bratislava, Slovakia Natl Inst Childrens Dis, Dept Paediat Neurol, Bratislava, Slovakia Comenius Univ, Fac Med, Bratislava, Slovakia
- [7] Phenotypic Spectrum of STXBP1 Gene Mutations in an Emirati Case SeriesCUREUS JOURNAL OF MEDICAL SCIENCE, 2023, 15 (09)Pawar, Nikhil论文数: 0 引用数: 0 h-index: 0机构: Al Jalila Childrens Special Hosp, Pediat Neurol, Dubai, U Arab Emirates Al Jalila Childrens Special Hosp, Pediat Neurol, Dubai, U Arab EmiratesMir, Fatima Farid论文数: 0 引用数: 0 h-index: 0机构: Dubai Hlth Author, Pediat, Dubai, U Arab Emirates Al Jalila Childrens Special Hosp, Pediat Neurol, Dubai, U Arab EmiratesTahir, Saja论文数: 0 引用数: 0 h-index: 0机构: Al Jalila Childrens Special Hosp, Pediat, Dubai, U Arab Emirates Al Jalila Childrens Special Hosp, Pediat Neurol, Dubai, U Arab EmiratesKashyape, Pawan论文数: 0 引用数: 0 h-index: 0机构: Al Jalila Childrens Special Hosp, Pediat Neurol, Dubai, U Arab Emirates Al Jalila Childrens Special Hosp, Pediat Neurol, Dubai, U Arab EmiratesBabiker, Mohamed O. E.论文数: 0 引用数: 0 h-index: 0机构: Al Jalila Childrens Special Hosp, Pediat Neurol, Dubai, U Arab Emirates Al Jalila Childrens Special Hosp, Pediat Neurol, Dubai, U Arab Emirates
- [8] Head stereotypies in STXBP1 encephalopathyDEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2013, 55 (08): : 769 - 772论文数: 引用数: h-index:机构:Korff, Christian M.论文数: 0 引用数: 0 h-index: 0机构: Univ Hosp Geneva, Paediat Neurol Child & Adolescent Dept, Geneva, Switzerland Univ Melbourne, Dept Med, Epilepsy Res Ctr, Austin Hlth, Melbourne, Vic, AustraliaVillaluz, Mel Michel G.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Dept Med, Epilepsy Res Ctr, Austin Hlth, Melbourne, Vic, Australia Univ Melbourne, Dept Med, Epilepsy Res Ctr, Austin Hlth, Melbourne, Vic, Australia论文数: 引用数: h-index:机构:Weckhuysen, Sarah论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neurogenet Lab, B-2020 Antwerp, Belgium Univ Melbourne, Dept Med, Epilepsy Res Ctr, Austin Hlth, Melbourne, Vic, AustraliaDe Jonghe, Peter论文数: 0 引用数: 0 h-index: 0机构: VIB, Dept Mol Genet, Neurogenet Grp, Antwerp, Belgium Univ Antwerp, Inst Born Bunge, Neurogenet Lab, B-2020 Antwerp, Belgium Univ Antwerp Hosp, Div Neurol, Antwerp, Belgium Univ Melbourne, Dept Med, Epilepsy Res Ctr, Austin Hlth, Melbourne, Vic, AustraliaScheffer, Ingrid E.论文数: 0 引用数: 0 h-index: 0机构: Univ Melbourne, Dept Med, Epilepsy Res Ctr, Austin Hlth, Melbourne, Vic, Australia Florey Inst, Melbourne, Vic, Australia Univ Melbourne, Royal Childrens Hosp, Dept Paediat, Melbourne, Vic, Australia Univ Melbourne, Dept Med, Epilepsy Res Ctr, Austin Hlth, Melbourne, Vic, Australia
- [9] Genotype-phenotype correlations of STXBP1 pathogenic variants and the treatment choices for STXBP1-related disorders in ChinaBMC MEDICAL GENOMICS, 2023, 16 (01)论文数: 引用数: h-index:机构:Chen, Baiyu论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R ChinaShan, Li-Dan论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R ChinaWang, Ying论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R ChinaYang, Lifen论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R ChinaYin, Fei论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R ChinaHe, Fang论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R ChinaPeng, Jing论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R ChinaWang, Guoli论文数: 0 引用数: 0 h-index: 0机构: Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China Hunan Intellectual & Dev Disabil Res Ctr, Changsha, Hunan, Peoples R China Cent South Univ, Xiangya Hosp, Dept Pediat, Changsha 410008, Hunan, Peoples R China
- [10] Haploinsufficiency of STXBP1 and Ohtahara syndromeEPILEPSIA, 2010, 51 : 71 - 71论文数: 引用数: h-index:机构:Kato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Dept Pediat, Fac Med, Yamagata 990, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Kanazawa Ku, Yokohama, Kanagawa 2360004, JapanMatsumoto, Naomichi论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Kanazawa Ku, Yokohama, Kanagawa 2360004, Japan