Possible Role of Mitochondrial Transfer RNA Gene 5816 A > G Genetic Polymorphism (m.5816A > G) in a 3-Year-Old Child with Dystonia: Report of a Case.

Wang, Sumei; Liang, Minglu; Ma, Jiehui; Huang, Sheng; Fan, Lili; Zhu, Feng; Sun, Dan

Wang, Sumei; Liang, Minglu; Ma, Jiehui; Huang, Sheng; Fan, Lili; Zhu, Feng; Sun, Dan.

Afiliação

Wang S; Department of Pediatric Neurology, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Liang M; Clinic Center of Human Gene Research, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Ma J; Department of Pediatric Neurology, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Huang S; Department of Pediatric Neurology, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Fan L; Department of Pediatric Neurology, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Zhu F; Clinic Center of Human Gene Research, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Sun D; Department of Pediatric Neurology, Wuhan Children's Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

Glob Med Genet ; 10(3): 263-270, 2023 Sep.

Article em En | MEDLINE | ID: mdl-37771542

Palavras-chave

dystonia; epilepsy; mitochondrial DNA mutation; mitochondrial diseases

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Glob Med Genet Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

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