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A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variant.
Ishihara, Naoko; Inagaki, Hidehito; Miyake, Misa; Kawamura, Yoshiki; Yoshikawa, Tetsushi; Kurahashi, Hiroki.
Afiliação
  • Ishihara N; Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
  • Inagaki H; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan.
  • Miyake M; Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
  • Kawamura Y; Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
  • Yoshikawa T; Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan.
  • Kurahashi H; Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan. Electronic address: kura@fujita-hu.ac.jp.
Brain Dev ; 41(3): 285-291, 2019 Mar.
Article em En | MEDLINE | ID: mdl-30392841
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: ATPase Trocadora de Sódio-Potássio / Epilepsia / Mutação Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: ATPase Trocadora de Sódio-Potássio / Epilepsia / Mutação Idioma: En Ano de publicação: 2019 Tipo de documento: Article