Leber's Hereditary Optic Neuropathy Is Associated with the T3866C Mutation in Mitochondrial ND1 Gene in Three Han Chinese Families

PURPOSE. To investigate the pathophysiology of Leber's hereditary optic neuropathy (LHON). METHODS. Seventy-one subjects from three Chinese families with LHON underwent clinical, genetic, molecular, and biochemical evaluations. Biochemical characterizations included the measurements of the rate...

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Detalhes bibliográficos
Main Authors: Zhou, Xiangtian, Qian, Yaping, Zhang, Juanjuan, Tong, Yi, Jiang, Pingping, Liang, Min, Dai, Xianning, Zhou, Huihui, Zhao, Fuxin, Ji, Yanchun, Mo, Jun Qin, Qu, Jia, Guan, Min-Xin
Formato: Artigo
Idioma:Inglês
Publicado em: The Association for Research in Vision and Ophthalmology 2012
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3394694/
https://ncbi.nlm.nih.gov/pubmed/22577081
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.11-9109
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