Mitochondrial 13513G>A Mutation With Low Mutant Load Presenting as Isolated Leber's Hereditary Optic Neuropathy Assessed by Next Generation Sequencing.

Sun, Chuan-Bin; Bai, Hai-Xia; Xu, Dan-Ni; Xiao, Qing; Liu, Zhe

Sun, Chuan-Bin; Bai, Hai-Xia; Xu, Dan-Ni; Xiao, Qing; Liu, Zhe.

Afiliação

Sun CB; Eye Center, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Bai HX; Eye Center, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Xu DN; Eye Center, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Xiao Q; Eye Center, Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, China.
Liu Z; Department of Ophthalmology, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, China.

Front Neurol ; 12: 601307, 2021.

Article em En | MEDLINE | ID: mdl-33746872

Palavras-chave

Leber's hereditary optic neuropathy; gene mutation; m13513G>A; mitochondrial DNA; optic atrophy

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Neurol Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China País de publicação: Suíça

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