A Chinese Family With Adult-Onset Leigh-Like Syndrome Caused by the Heteroplasmic m.10191T>C Mutation in the Mitochondrial MTND3 Gene.

Li, Tao-Ran; Wang, Qun; Liu, Mao-Mao; Lv, Rui-Juan

Li, Tao-Ran; Wang, Qun; Liu, Mao-Mao; Lv, Rui-Juan.

Afiliação

Li TR; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, China National Clinical Research Center for Neurological Diseases, Beijing, China.
Wang Q; Department of Neurology, XuanWu Hospital of Capital Medical University, Beijing, China.
Liu MM; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, China National Clinical Research Center for Neurological Diseases, Beijing, China.
Lv RJ; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, China National Clinical Research Center for Neurological Diseases, Beijing, China.

Front Neurol ; 10: 347, 2019.

Article em En | MEDLINE | ID: mdl-31105631

Palavras-chave

Leigh syndrome; Leigh-like syndrome; MELAS; MELAS-LS overlap syndrome; m.10191T>C mutation

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Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Front Neurol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China