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Abnormal axonal development and severe epileptic phenotype in Dynamin-1 (DNM1) encephalopathy.
Matsubara, Kohei; Kuki, Ichiro; Ishioka, Risako; Yamada, Naoki; Fukuoka, Masataka; Inoue, Takeshi; Nukui, Megumi; Okamoto, Nobuhiko; Mizuguchi, Takeshi; Matsumoto, Naomichi; Okazaki, Shin.
  • Matsubara K; Division of Pediatric Neurology, Osaka City General Hospital, Osaka, Japan.
  • Kuki I; Division of Pediatric Neurology, Osaka City General Hospital, Osaka, Japan.
  • Ishioka R; Division of Pediatric Neurology, Osaka City General Hospital, Osaka, Japan.
  • Yamada N; Division of Pediatric Neurology, Osaka City General Hospital, Osaka, Japan.
  • Fukuoka M; Division of Pediatric Neurology, Osaka City General Hospital, Osaka, Japan.
  • Inoue T; Division of Pediatric Neurology, Osaka City General Hospital, Osaka, Japan.
  • Nukui M; Division of Pediatric Neurology, Osaka City General Hospital, Osaka, Japan.
  • Okamoto N; Division of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, Japan.
  • Mizuguchi T; Division of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Matsumoto N; Division of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Okazaki S; Division of Pediatric Neurology, Osaka City General Hospital, Osaka, Japan.
Epileptic Disord ; 26(1): 139-143, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38009673
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espasmos Infantiles / Encefalopatías / Epilepsia Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Espasmos Infantiles / Encefalopatías / Epilepsia Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article