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MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNAMet gene.
Kuwajima, Mari; Goto, Masahide; Kurane, Koyuru; Shimbo, Hiroko; Omika, Narumi; Jimbo, Eriko F; Muramatsu, Kazuhiro; Tajika, Makiko; Shimura, Masaru; Murayama, Kei; Kurosawa, Kenji; Yamagata, Takanori; Osaka, Hitoshi.
Afiliación
  • Kuwajima M; Department of Pediatrics, Jichi Medical University, Japan.
  • Goto M; Department of Pediatrics, Jichi Medical University, Japan.
  • Kurane K; Department of Pediatrics, Jichi Medical University, Japan.
  • Shimbo H; Department of Genetics, Kanagawa Children's Medical Center, Yokohama, Kanagawa, Japan.
  • Omika N; Department of Pediatrics, Jichi Medical University, Japan.
  • Jimbo EF; Department of Pediatrics, Jichi Medical University, Japan.
  • Muramatsu K; Department of Pediatrics, Jichi Medical University, Japan.
  • Tajika M; Department of Metabolism, Chiba Children's Hospital, Japan.
  • Shimura M; Department of Metabolism, Chiba Children's Hospital, Japan.
  • Murayama K; Department of Metabolism, Chiba Children's Hospital, Japan.
  • Kurosawa K; Department of Genetics, Kanagawa Children's Medical Center, Yokohama, Kanagawa, Japan.
  • Yamagata T; Department of Pediatrics, Jichi Medical University, Japan.
  • Osaka H; Department of Pediatrics, Jichi Medical University, Japan. Electronic address: hosaka@jichi.ac.jp.
Brain Dev ; 41(5): 465-469, 2019 May.
Article en En | MEDLINE | ID: mdl-30739820

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ARN de Transferencia de Metionina / Síndrome MELAS / ARN Mitocondrial Límite: Child / Female / Humans Idioma: En Revista: Brain Dev Año: 2019 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: ARN de Transferencia de Metionina / Síndrome MELAS / ARN Mitocondrial Límite: Child / Female / Humans Idioma: En Revista: Brain Dev Año: 2019 Tipo del documento: Article País de afiliación: Japón