Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure
スポンサーリンク
概要
- 論文の詳細を見る
- 2013-05-01
著者
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NIIHORI Tetsuya
Department of Medical Genetics, Tohoku University School of Medicine
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Tateyama Maki
Department Of Neurology Tohoku University School Of Medicine
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Matsubara Yoichi
Department Of Medical Genetics Tohoku University Of Graduate School Of Medicine
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Kato Masaaki
Department Of Cardiovascular Surgery Morinomiya Hospital
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Nakayama Keiko
Division Of Abdominal Ultrasound Kobe City General Hospital
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Takahashi Toshiaki
Department Of Anesthesiology Tokyo Medical University
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Abe Koji
Department Of Applied Chemistry Graduate School Of Engineering Tohoku University
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Warita Hitoshi
Department Of Neurology Tohoku University School Of Medicine
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Aoki Masashi
Department of Electrical and Electronic Engineering, National Defense Academy, 1-10-20 Hashirimizu, Yokosuka, Kanagawa 239-8686, Japan
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Izumi Rumiko
Department of Neurology, Tohoku University School of Medicine, Japan
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AOKI Yoko
Department of Food and Nutrition, Japan Women's University
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SUZUKI Naoki
Department of Agricultural Chemistry, Ibaraki University
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ABE Koji
Department of Neurology, Okayama University Medical School
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NAGASHIMA Takeshi
Division of Cell Proliferation, United Centers for Advanced Research and Translational Medicine, Tohoku University Graduate School of Medicine
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FUNAYAMA Ryo
Division of Cell Proliferation, United Centers for Advanced Research and Translational Medicine, Tohoku University Graduate School of Medicine
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IZUMI Rumiko
Department of Medical Genetics, Tohoku University School of Medicine
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NAKAYAMA Keiko
Division of Cell Proliferation, United Centers for Advanced Research and Translational Medicine, Tohoku University Graduate School of Medicine
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