Missense mutation of the sodium channel gene SCN2A causes Dravet syndrome

• SHI Xiuyu

  Department of Pediatrics, School of Medicine, Fukuoka University

• YASUMOTO Sawa

  Department of Pediatrics, School of Medicine, Fukuoka University

• NAKAGAWA Eiji

  Department of Pediatric Neurology, Musashi Hospital, National Center of Neurology and Psychiatry

• FUKASAWA Tatsuya

  Department of Pediatrics, Nagoya Memorial Hospital

• UCHIYA Satoshi

  Department of Pediatrics, Mito Saiseikai General Hospital

• HIROSE Shinichi

  Department of Pediatrics, School of Medicine, Fukuoka University

収録刊行物

• Brain & development

  Brain & development 31 (10), 758-762, 2009-11-01

キーワード

• Dravet syndrome
• SCN1A
• SCN2A
• GABRG2
• Genetics

詳細情報

• CRID: 1571980075946968192
• NII論文ID: 10026413050
• NII書誌ID: AA00111153
• ISSN: 03877604
• Web Site: https://search.jamas.or.jp/link/ui/2010127756
• 本文言語コード: en
• データソース種別:
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