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Late-onset Leigh syndrome with m.9176T>C mutation in the mitochondrial ATPase 6 gene.
Ichikawa, Kazushi; Tsuyusaki, Yu; Shimbo, Hiroko; Goto, Tomohide.
Affiliation
  • Ichikawa K; Division of Neurology, Kanagawa Children's Medical Center, Yokohama, Kanagawa, Japan.
  • Tsuyusaki Y; Division of Neurology, Kanagawa Children's Medical Center, Yokohama, Kanagawa, Japan.
  • Shimbo H; Division of Neurology, Clinical Research Institute, Kanagawa Children's Medical Center, Yokohama, Kanagawa, Japan.
  • Goto T; Division of Neurology, Kanagawa Children's Medical Center, Yokohama, Kanagawa, Japan.
Pediatr Int ; 61(10): 1055-1056, 2019 Oct.
Article in En | MEDLINE | ID: mdl-31625254
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Full text: 1 Database: MEDLINE Main subject: Leigh Disease / Mitochondrial Proton-Translocating ATPases / Mutation Limits: Child / Humans / Male Language: En Journal: Pediatr Int Journal subject: PEDIATRIA Year: 2019 Type: Article Affiliation country: Japan
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Leigh Disease / Mitochondrial Proton-Translocating ATPases / Mutation Limits: Child / Humans / Male Language: En Journal: Pediatr Int Journal subject: PEDIATRIA Year: 2019 Type: Article Affiliation country: Japan