Symposium
Sat. May 22, 2021 8:00 AM - 10:00 AM Room 10 (ICC Kyoto 1F Swan Hall)
Chair：Naoki Atsuta (Department of Neurology, Aichi Medical University School of Medicine, Japan / Department of Neurology, Nagoya University Graduate School of Medicine, Japan)
疾患のゲノム背景を読み解くことは、疾患病態解明や治療開発への有用な情報となりうる。本シンポジウムでは、近年進歩が著しい、孤発性・家族性神経疾患のゲノム研究の中から、認知症・パーキンソン病・脊髄小脳変性症・筋萎縮性側索硬化症・希少疾患を取り上げた。神経ゲノム研究の現状と今後を考える良い機会になると考えられる。
○Satoko Miyatake (Clinical Genetics Department, Yokohama City University Hospital, Japan)
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○Wataru Satake1, Pei Chieng Cha2, Takeshi Uenaka2, Tatsushi Toda1 (1.Dept Neurol, Japan, 2.Dept Neurol/Mol Bra Sci)
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○Naoki Atsuta1,2, Ryoichi Nakamura2, Genki Tohnai2, Gen Sobue3 (1.Department of Neurology, Aichi Medical University School of Medicine, Japan, 2.Department of Neurology, Nagoya University Graduate School of Medicine, Japan, 3.Aichi Medical University School of Medicine)
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○Shumpei Niida (National Center for Geriatrics and Gerontology, Japan)
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○Shinichi Morishita (University of Tokyo, Japan)
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