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A case of recurrent encephalopathy with SCN2A missense mutation.
Fukasawa, Tatsuya; Kubota, Tetsuo; Negoro, Tamiko; Saitoh, Makiko; Mizuguchi, Masashi; Ihara, Yukiko; Ishii, Atsushi; Hirose, Shinichi.
  • Fukasawa T; Department of Pediatrics, Anjo Kosei Hospital, Aichi, Japan. Electronic address: fukasawa@kosei.anjo.aichi.jp.
  • Kubota T; Department of Pediatrics, Anjo Kosei Hospital, Aichi, Japan.
  • Negoro T; Department of Pediatrics, Anjo Kosei Hospital, Aichi, Japan.
  • Saitoh M; Department of Developmental Medical Sciences, Graduate School of Medicine, University of Tokyo, Japan.
  • Mizuguchi M; Department of Developmental Medical Sciences, Graduate School of Medicine, University of Tokyo, Japan.
  • Ihara Y; Department of Pediatrics, School of Medicine, Fukuoka University, Fukuoka, Japan.
  • Ishii A; Department of Pediatrics, School of Medicine, Fukuoka University, Fukuoka, Japan.
  • Hirose S; Department of Pediatrics, School of Medicine, Fukuoka University, Fukuoka, Japan.
Brain Dev ; 37(6): 631-4, 2015 Jun.
Article en En | MEDLINE | ID: mdl-25457084
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Encefalopatías / Mutación Missense / Canal de Sodio Activado por Voltaje NAV1.2 Límite: Humans / Infant / Male Idioma: En Año: 2015 Tipo del documento: Article
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Encefalopatías / Mutación Missense / Canal de Sodio Activado por Voltaje NAV1.2 Límite: Humans / Infant / Male Idioma: En Año: 2015 Tipo del documento: Article