Myoclonic epilepsy with ragged red fibers syndrome associated with mitochondrial 3302A>G mutation in the MT­TL1 gene: A case report.

Huang, Gang; Wang, Yanmei; Yao, Dongyuan

Myoclonic epilepsy with ragged red fibers syndrome associated with mitochondrial 3302A>G mutation in the MTTL1 gene: A case report.

Huang, Gang; Wang, Yanmei; Yao, Dongyuan.

Afiliação

Huang G; Department of Neurology, Jiangxi Provincial People's Hospital and The First Affiliated Hospital of Nanchang Medical College, Nanchang, Jiangxi 330006, P.R. China.
Wang Y; Neurological Institute of Jiangxi Province, Jiangxi Provincial People's Hospital and The First Affiliated Hospital of Nanchang Medical College, Nanchang, Jiangxi 330006, P.R. China.
Yao D; Department of Neurology, Jiangxi Provincial People's Hospital and The First Affiliated Hospital of Nanchang Medical College, Nanchang, Jiangxi 330006, P.R. China.

Exp Ther Med ; 25(2): 87, 2023 Feb.

Article em En | MEDLINE | ID: mdl-36684660

Palavras-chave

MT-TL1 gene; gene mutation; mitochondrial DNA; mitochondrial encephalomyopathy; myoclonic epilepsy with ragged red fibers syndrome

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Exp Ther Med Ano de publicação: 2023 Tipo de documento: Article

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