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Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation.
Xu, Xue-Bi; Ji, Kun-Qian; Lyu, Jing-Wei; Zhang, Shu; Lyu, Xiao-Qing; Liu, Chang; Li, Wei; Yan, Chuan-Zhu; Zhao, Yu-Ying.
Afiliación
  • Xu XB; Research Institute of Neuromuscular and Neurodegenerative Diseases and Department of Neurology, Qilu Hospital, Shandong University, Jinan, Shandong 250000, China.
  • Ji KQ; Brain Science Research Institute, Shandong University, Jinan, Shandong 250000, China.
  • Lyu JW; Research Institute of Neuromuscular and Neurodegenerative Diseases and Department of Neurology, Qilu Hospital, Shandong University, Jinan, Shandong 250000, China.
  • Zhang S; Brain Science Research Institute, Shandong University, Jinan, Shandong 250000, China.
  • Lyu XQ; Research Institute of Neuromuscular and Neurodegenerative Diseases and Department of Neurology, Qilu Hospital, Shandong University, Jinan, Shandong 250000, China.
  • Liu C; Brain Science Research Institute, Shandong University, Jinan, Shandong 250000, China.
  • Li W; Research Institute of Neuromuscular and Neurodegenerative Diseases and Department of Neurology, Qilu Hospital, Shandong University, Jinan, Shandong 250000, China.
  • Yan CZ; Research Institute of Neuromuscular and Neurodegenerative Diseases and Department of Neurology, Qilu Hospital, Shandong University, Jinan, Shandong 250000, China.
  • Zhao YY; Research Institute of Neuromuscular and Neurodegenerative Diseases and Department of Neurology, Qilu Hospital, Shandong University, Jinan, Shandong 250000, China.
Chin Med J (Engl) ; 132(6): 716-718, 2019 03 20.
Article en En | MEDLINE | ID: mdl-30741831
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Mitocondrial / Síndrome MELAS Límite: Humans / Male / Middle aged Idioma: En Revista: Chin Med J (Engl) Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: China
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: ADN Mitocondrial / Síndrome MELAS Límite: Humans / Male / Middle aged Idioma: En Revista: Chin Med J (Engl) Año: 2019 Tipo del documento: Article País de afiliación: China Pais de publicación: China