Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation
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概要
- 論文の詳細を見る
- 2000-03-01
著者
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MATSUO Masafumi
Division of Molecular Medicine, Department of International and Environmental Medical Science
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Surono Agus
Division Of Genetics International Center For Medical Research Kobe University School Of Medicine
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WIBAWA Tri
Division of Genetics, International Center for Medical Research, Kobe University School of Medicine
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TAKASHIMA Yasuhiro
Department of Pediatrics, Kobe University School of Medicine
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MITSUYOSHI Izuru
Department of Pediatrics, National Utano Hospital
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WADA Hiroko
Department of Pediatrics, Sakura Ryoikuen Hospital
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NAKAMURA Hajime
Department of Pediatrics, Kobe University School of Medicine
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Wibawa Tri
Division Of Genetics International Center For Medical Research Kobe University School Of Medicine
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Wada Hiroko
Division Of Pediatrics Department Of Development And Aging Kobe University School Of Medicine
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Nakamura Hajime
Hyogo Prefectural Kobe Children's Hospital
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Mitsuyoshi Izuru
Department Of Pediatrics National Utano Hospital
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Mitsuyoshi Izuru
Department Of Pediatrics Kansai Regional Epilepsy Center National Utano Hospital
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Takashima Yasuhiro
Department Of Information And Media The University Of Kitakyushu
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Nakamura H
Hyogo Prefectural Kobe Children's Hospital
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Wada Hiroko
Department Of Applied Chemistry Nagoya Insitute Of Technology
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Mizutori Masakazu
Department Of Pediatrics Graduate School Of Medicine Kobe University
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Matsuo Masafumi
Division Of Genetics Icmr Kobe University
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Nakamura Hajime
Department Of Biological Responses Institute For Virus Research Kyoto University
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Yamasaki Takemi
Hyogo Prefectural Children's Hospital
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Takeshima Y
Hyogo Prefectural Children's Hospital
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Nakamura Hajime
Department Of Development And Aging Faculty Of Medicine Kobe University Graduate School Of Medicine
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