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Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathy.
Ma, Yan-Yan; Wu, Tong-Fei; Liu, Yu-Peng; Wang, Qiao; Li, Xi-Yuan; Ding, Yuan; Song, Jin-Qing; Shi, Xiu-Yu; Zhang, Wei-Na; Zhao, Meng; Hu, Ling-Yan; Ju, Jun; Wang, Zhi-Long; Yang, Yan-Ling; Zou, Li-Ping.
Afiliación
  • Ma YY; Department of Pediatrics, Chinese Liberation Army General Hospital, Beijing, PR China.
  • Wu TF; Department of Pediatrics, Peking University First Hospital, Beijing, PR China.
  • Liu YP; Department of Pediatrics, Peking University First Hospital, Beijing, PR China.
  • Wang Q; Department of Pediatrics, Peking University First Hospital, Beijing, PR China.
  • Li XY; Department of Pediatrics, Peking University First Hospital, Beijing, PR China.
  • Ding Y; Department of Pediatrics, Peking University First Hospital, Beijing, PR China.
  • Song JQ; Department of Pediatrics, Peking University First Hospital, Beijing, PR China.
  • Shi XY; Department of Pediatrics, Chinese Liberation Army General Hospital, Beijing, PR China.
  • Zhang WN; Department of Pediatrics, Chinese Liberation Army General Hospital, Beijing, PR China.
  • Zhao M; Department of Pediatrics, Chinese Liberation Army General Hospital, Beijing, PR China.
  • Hu LY; Department of Pediatrics, Chinese Liberation Army General Hospital, Beijing, PR China.
  • Ju J; Department of Pediatrics, Chinese Liberation Army General Hospital, Beijing, PR China.
  • Wang ZL; Clinical Laboratory of Zhongke, Beijing, PR China.
  • Yang YL; Department of Pediatrics, Peking University First Hospital, Beijing, PR China. Electronic address: amino_acid3003@126.com.
  • Zou LP; Department of Pediatrics, Chinese Liberation Army General Hospital, Beijing, PR China. Electronic address: zouliping21@hotmail.com.
Brain Dev ; 36(5): 394-8, 2014 May.
Article en En | MEDLINE | ID: mdl-23849264
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mutación del Sistema de Lectura / Enfermedades Mitocondriales / Complejo II de Transporte de Electrones / Errores Innatos del Metabolismo Tipo de estudio: Diagnostic_studies Límite: Child / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Brain Dev Año: 2014 Tipo del documento: Article Pais de publicación: Países Bajos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mutación del Sistema de Lectura / Enfermedades Mitocondriales / Complejo II de Transporte de Electrones / Errores Innatos del Metabolismo Tipo de estudio: Diagnostic_studies Límite: Child / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Brain Dev Año: 2014 Tipo del documento: Article Pais de publicación: Países Bajos