Extended spinal cord involvement in adult-onset Leigh syndrome due to mitochondrial 10197G > A mutation.

Wei, Yanping; Qian, Min; Yang, Yingmai

Wei, Yanping; Qian, Min; Yang, Yingmai.

Afiliación

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 en En | MEDLINE | ID: mdl-35907985

Asunto(s)

Enfermedad de Leigh; Atrofias Ópticas Hereditarias; Humanos; Adulto; Enfermedad de Leigh/diagnóstico por imagen; Enfermedad de Leigh/genética; Mutación/genética; Médula Espinal/diagnóstico por imagen; ADN Mitocondrial/genética

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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Enfermedad de Leigh / Atrofias Ópticas Hereditarias Idioma: En Revista: Neurol Sci Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article

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