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Establishment of a human induced stem cell line (FUi002-A) from Dravet syndrome patient carrying heterozygous R1525X mutation in SCN1A gene.
Tanaka, Yasuyoshi; Higurashi, Norimichi; Shirasu, Naoto; Yasunaga, Shin'ichiro; Moreira, Kevin Mello; Okano, Hideyuki; Hirose, Shinichi.
Afiliação
  • Tanaka Y; Central Research Institute for the Molecular Pathomechanisms of Epilepsy, Fukuoka University, Japan.
  • Higurashi N; Department of Pediatrics, Jikei University School of Medicine, Japan.
  • Shirasu N; Department of Biochemistry, School of Medicine, Fukuoka University, Japan.
  • Yasunaga S; Department of Biochemistry, School of Medicine, Fukuoka University, Japan.
  • Moreira KM; Department of Pediatrics, School of Medicine, Fukuoka University, Japan.
  • Okano H; Department of Physiology, Keio University School of Medicine, Japan.
  • Hirose S; Central Research Institute for the Molecular Pathomechanisms of Epilepsy, Fukuoka University, Japan; Department of Pediatrics, School of Medicine, Fukuoka University, Japan. Electronic address: hirose@fukuoka-u.ac.jp.
Stem Cell Res ; 31: 11-15, 2018 08.
Article em En | MEDLINE | ID: mdl-29981888
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Mioclônicas / Canal de Sódio Disparado por Voltagem NAV1.1 Limite: Adult / Humans / Male Idioma: En Revista: Stem Cell Res Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsias Mioclônicas / Canal de Sódio Disparado por Voltagem NAV1.1 Limite: Adult / Humans / Male Idioma: En Revista: Stem Cell Res Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão