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- [1] Protein, and mRNABased phenotype-genotype correlations in DMD/DMD with point mutations and molecular basis for BMD with nonsense and frameshift mutations in the DMD geneHUMAN MUTATION, 2007, 28 (02) : 183 - 195Deburgrave, Nathalie论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceDaoud, Fatma论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceLlense, Stehane论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceBarbot, Jean Claude论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceRecan, Dominique论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FrancePeccate, Cecile论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceBurghes, Arthur H. M.论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceBeroud, Christophe论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceGarcia, Luis论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceKaplan, JeanClaude论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceChelly, Jamel论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, FranceLeturcq, France论文数: 0 引用数: 0 h-index: 0机构: Univ Paris 05, INSERM, Inst Cochin, Unite 567,CNR UMR 1408,UM3, Paris, France
- [2] Two closely spaced nonsense mutations in the DMD gene in a Malaysian familyMOLECULAR GENETICS AND METABOLISM, 2011, 103 (03) : 303 - 304Rani, Abdul Qawee论文数: 0 引用数: 0 h-index: 0机构: Univ Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kelantan, Malaysia Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanMalueka, Rusdy Ghazali论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanSasongko, Teguh Haryo论文数: 0 引用数: 0 h-index: 0机构: Univ Sains Malaysia, Ctr Human Genome, Sch Med Sci, Kelantan, Malaysia Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanAwano, Hiroyuki论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanLee, Tomoko论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanYagi, Mariko论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanZilfalil, Bin Alwi论文数: 0 引用数: 0 h-index: 0机构: Univ Sains Malaysia, Dept Pediat, Sch Med Sci, Kelantan, Malaysia Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanSalmi, A. B. Razak论文数: 0 引用数: 0 h-index: 0机构: Univ Sains Malaysia, Dept Pediat, Sch Med Sci, Kelantan, Malaysia Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanTakeshima, Yasuhiro论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanZabidi-Hussin, Z. A. M. H.论文数: 0 引用数: 0 h-index: 0机构: Univ Sains Malaysia, Dept Pediat, Sch Med Sci, Kelantan, Malaysia Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, JapanMatsuo, Masafumi论文数: 0 引用数: 0 h-index: 0机构: Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, Japan Kobe Univ, Grad Sch Med, Dept Pediat, Chuo Ku, Kobe, Hyogo 6500017, Japan
- [3] Clinical, pathological and molecular findings in nemaline myopathy cases caused by mutations in the skeletal muscle actin geneJOURNAL OF INVESTIGATIVE MEDICINE, 2003, 51 : S386 - S387Strickland, CD论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Pediat, Boston, MA 02115 USA Childrens Hosp, Dept Pediat, Boston, MA 02115 USAMidgett, C论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Pediat, Boston, MA 02115 USA Childrens Hosp, Dept Pediat, Boston, MA 02115 USARyan, M论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Pediat, Boston, MA 02115 USA Childrens Hosp, Dept Pediat, Boston, MA 02115 USAPoulos, MA论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Pediat, Boston, MA 02115 USA Childrens Hosp, Dept Pediat, Boston, MA 02115 USANewburger, DE论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Pediat, Boston, MA 02115 USA Childrens Hosp, Dept Pediat, Boston, MA 02115 USABeggs, AH论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp, Dept Pediat, Boston, MA 02115 USA Childrens Hosp, Dept Pediat, Boston, MA 02115 USA
- [4] Mutations in progranulin gene:: Clinical, pathological, and ribonucleic acid expression findingsBIOLOGICAL PSYCHIATRY, 2008, 63 (10) : 946 - 952de Munain, Adolofo Lopez论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Unidad Expt, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainAlzualde, Ainhoa论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Unidad Expt, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainGorostidi, Ana论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Unidad Expt, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainOtaegui, David论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Unidad Expt, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainRuiz-Martinez, Javier论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Mendaro, Serv Neurol, Mendaro, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainIndakoetxea, Begona论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainFerrer, Isidro论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ Bellvitge, Hosp Llobregat, Inst Neuropatol, Barcelona, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainPerez-Tur, Jordi论文数: 0 引用数: 0 h-index: 0机构: CSIC, Inst BIOmed Valencia, Unitat Genet Mol, Valencia, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainSaenz, Amets论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Unidad Expt, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainBergareche, Alberto论文数: 0 引用数: 0 h-index: 0机构: Hosp Bidasoa, Serv Neurol, Hondarribia, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainBarandiaran, Miriam论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainPoza, Juan Jose论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainZabalza, Ramon论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainRuiz, Irune论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Anat Patol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainUrtasun, Miguel论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainFernandez-Manchola, Inaki论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainOlasagasti, Bixen论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainEspinal, Juan Bautista论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainOlaskoaga, Javier论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainRuibal, Marta论文数: 0 引用数: 0 h-index: 0机构: Hosp Ntra Sra Antigua, Zumarraga, Gipuzkoa, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainMoreno, Fermin论文数: 0 引用数: 0 h-index: 0机构: Hosp Ntra Sra Antigua, Zumarraga, Gipuzkoa, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainCarrera, Nieves论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, SpainMasso, Jose Felix Marti论文数: 0 引用数: 0 h-index: 0机构: Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain Hosp Donostia, Dept Neurol, Serv Neurol, San Sabastian 20014, Spain
- [5] The position of nonsense mutations can predict the phenotype severity: A survey on the DMD genePLOS ONE, 2020, 15 (08):Torella, Annalaura论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy Telethon Inst Genet & Med TIGEM, Pozzuoli, Italy Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, ItalyZanobio, Mariateresa论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, ItalyZeuli, Roberta论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, ItalyBlanco, Francesca del Vecchio论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, ItalySavarese, Marco论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy Univ Helsinki, Folkhalsan Res Ctr, Med, Helsinki, Finland Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, ItalyGiugliano, Teresa论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, ItalyGarofalo, Arcomaria论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, ItalyPiluso, Giulio论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, ItalyPolitano, Luisa论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Sperimentale, Naples, Italy Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, ItalyNigro, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy Telethon Inst Genet & Med TIGEM, Pozzuoli, Italy Univ Campania Luigi Vanvitelli, Dipartimento Med Precis, Naples, Italy
- [6] Clinical and molecular characterisation of unusual DMD mutationsNEUROMUSCULAR DISORDERS, 2021, 31 : S79 - S79Nicolau, S.论文数: 0 引用数: 0 h-index: 0机构: Nationwide Childrens Hosp, Columbus, OH USA Nationwide Childrens Hosp, Columbus, OH USAVetter, T.论文数: 0 引用数: 0 h-index: 0机构: Nationwide Childrens Hosp, Columbus, OH USA Nationwide Childrens Hosp, Columbus, OH USABradley, A.论文数: 0 引用数: 0 h-index: 0机构: Nationwide Childrens Hosp, Columbus, OH USA Nationwide Childrens Hosp, Columbus, OH USAFrair, E.论文数: 0 引用数: 0 h-index: 0机构: Nationwide Childrens Hosp, Columbus, OH USA Nationwide Childrens Hosp, Columbus, OH USAWeiss, R.论文数: 0 引用数: 0 h-index: 0机构: Univ Utah, Salt Lake City, UT USA Nationwide Childrens Hosp, Columbus, OH USAFlanigan, K.论文数: 0 引用数: 0 h-index: 0机构: Nationwide Childrens Hosp, Columbus, OH USA Nationwide Childrens Hosp, Columbus, OH USA
- [7] BMD phenotypes from 'DMD' mutations: Molecular mechanisms of phenotypic amelioration of mutations in the DMD geneNEUROLOGY, 2007, 68 (12) : A1 - A1Flanigan, Kevin论文数: 0 引用数: 0 h-index: 0Gurvich, Olga论文数: 0 引用数: 0 h-index: 0Anderson, Chris论文数: 0 引用数: 0 h-index: 0Hart, Kim论文数: 0 引用数: 0 h-index: 0Weiss, Robert论文数: 0 引用数: 0 h-index: 0Howard, Michael T.论文数: 0 引用数: 0 h-index: 0
- [8] Application whole exome sequencing for the clinical molecular diagnosis of patients with Duchenne muscular dystrophy; identification of four novel nonsense mutations in four unrelated Chinese DMD patientsMOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 7 (05):Zhang, Yan论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaYang, Weikang论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Prevent & Hlth Care, Shenzhen, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaWen, Guoming论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Outpatient, Shenzhen, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaWu, Yanxia论文数: 0 引用数: 0 h-index: 0机构: Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou, Guangdong, Peoples R China Southern Med Univ, Sch Basic Med Sci, Guangzhou, Guangdong, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaJing, Zhiliang论文数: 0 引用数: 0 h-index: 0机构: Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou, Guangdong, Peoples R China Southern Med Univ, Sch Basic Med Sci, Guangzhou, Guangdong, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaLi, Dazhou论文数: 0 引用数: 0 h-index: 0机构: Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou, Guangdong, Peoples R China Southern Med Univ, Sch Basic Med Sci, Guangzhou, Guangdong, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaTang, Minshan论文数: 0 引用数: 0 h-index: 0机构: Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou, Guangdong, Peoples R China Southern Med Univ, Sch Basic Med Sci, Guangzhou, Guangdong, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaLiu, Guanglong论文数: 0 引用数: 0 h-index: 0机构: Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou, Guangdong, Peoples R China Southern Med Univ, Sch Basic Med Sci, Guangzhou, Guangdong, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaWe, Xuxuan论文数: 0 引用数: 0 h-index: 0机构: Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou, Guangdong, Peoples R China Southern Med Univ, Sch Basic Med Sci, Guangzhou, Guangdong, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaZhong, Yan论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaLi, Yanhua论文数: 0 引用数: 0 h-index: 0机构: Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R ChinaDeng, Yongjian论文数: 0 引用数: 0 h-index: 0机构: Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou, Guangdong, Peoples R China Southern Med Univ, Sch Basic Med Sci, Guangzhou, Guangdong, Peoples R China Shenzhen Longhua Dist Matern & Child Healthcare H, Dept Pathol, Shenzhen, Peoples R China
- [9] Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophyHuman Genetics, 2020, 139 : 247 - 255Mariko Okubo论文数: 0 引用数: 0 h-index: 0机构: National Center of Neurology and Psychiatry,Department of Neuromuscular Research, National Institute of NeuroscienceSatoru Noguchi论文数: 0 引用数: 0 h-index: 0机构: National Center of Neurology and Psychiatry,Department of Neuromuscular Research, National Institute of NeuroscienceShinichiro Hayashi论文数: 0 引用数: 0 h-index: 0机构: National Center of Neurology and Psychiatry,Department of Neuromuscular Research, National Institute of NeuroscienceHarumasa Nakamura论文数: 0 引用数: 0 h-index: 0机构: National Center of Neurology and Psychiatry,Department of Neuromuscular Research, National Institute of NeuroscienceHirofumi Komaki论文数: 0 引用数: 0 h-index: 0机构: National Center of Neurology and Psychiatry,Department of Neuromuscular Research, National Institute of NeuroscienceMasafumi Matsuo论文数: 0 引用数: 0 h-index: 0机构: National Center of Neurology and Psychiatry,Department of Neuromuscular Research, National Institute of NeuroscienceIchizo Nishino论文数: 0 引用数: 0 h-index: 0机构: National Center of Neurology and Psychiatry,Department of Neuromuscular Research, National Institute of Neuroscience
- [10] Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophyHUMAN GENETICS, 2020, 139 (02) : 247 - 255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:Nakamura, Harumasa论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Translat Med Ctr, Dept Promoting Clin Trial & Translat Med, Tokyo, Japan Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Neuromuscular Res, 4-1-1 Ogawa Higashi, Kodaira, Tokyo 1878502, JapanKomaki, Hirofumi论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Translat Med Ctr, Tokyo, Japan Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Neuromuscular Res, 4-1-1 Ogawa Higashi, Kodaira, Tokyo 1878502, JapanMatsuo, Masafumi论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Neurol & Psychiat, Fac Rehabil, KNC Dept Nucle Acid Drug Discovery, Kobe, Hyogo, Japan Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Neuromuscular Res, 4-1-1 Ogawa Higashi, Kodaira, Tokyo 1878502, Japan论文数: 引用数: h-index:机构: