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Siblings with optic neuropathy and RTN4IP1 mutation.
Okamoto, Nobuhiko; Miya, Fuyuki; Hatsukawa, Yoshikazu; Suzuki, Yasuhiro; Kawato, Kazumi; Yamamoto, Yuto; Tsunoda, Tatsuhiko; Kato, Mitsuhiro; Saitoh, Shinji; Yamasaki, Mami; Kanemura, Yonehiro; Kosaki, Kenjiro.
Afiliación
  • Okamoto N; Department of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, Japan.
  • Miya F; Department of Medical Science Mathematics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
  • Hatsukawa Y; Laboratory for Medical Science Mathematics, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
  • Suzuki Y; Department of Ophthalmology, Osaka Women's and Children's Hospital, Osaka, Japan.
  • Kawato K; Department of Pediatric Neurology, Osaka Medical Center and Research Institute for Maternal and Child Health, Osaka, Japan.
  • Yamamoto Y; Department of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, Japan.
  • Tsunoda T; Department of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, Japan.
  • Kato M; Department of Medical Science Mathematics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
  • Saitoh S; Laboratory for Medical Science Mathematics, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan.
  • Yamasaki M; Department of Pediatrics, Showa University School of Medicine, Tokyo, Japan.
  • Kanemura Y; Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Kosaki K; Department of Pediatric Neurosurgery, Takatsuki General Hospital, Osaka, Japan.
J Hum Genet ; 62(10): 927-929, 2017 Oct.
Article en En | MEDLINE | ID: mdl-28638143
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Portadoras / Enfermedades del Nervio Óptico / Proteínas Mitocondriales / Hermanos / Mutación Límite: Adolescent / Humans / Male Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Japón
Texto completo
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Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Portadoras / Enfermedades del Nervio Óptico / Proteínas Mitocondriales / Hermanos / Mutación Límite: Adolescent / Humans / Male Idioma: En Revista: J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Japón