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Extended spinal cord involvement in adult-onset Leigh syndrome due to mitochondrial 10197G > A mutation.
Wei, Yanping; Qian, Min; Yang, Yingmai.
Afiliação
  • Wei Y; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing Shuaifuyuan 1, Dongcheng District, Beijing, 100730, People's Republic of China. yp924@sina.com.
  • Qian M; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing Shuaifuyuan 1, Dongcheng District, Beijing, 100730, People's Republic of China.
  • Yang Y; Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing Shuaifuyuan 1, Dongcheng District, Beijing, 100730, People's Republic of China.
Neurol Sci ; 43(12): 6997-7000, 2022 12.
Article em En | MEDLINE | ID: mdl-35907985
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Leigh / Atrofias Ópticas Hereditárias Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Leigh / Atrofias Ópticas Hereditárias Idioma: En Ano de publicação: 2022 Tipo de documento: Article