Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese

PURPOSE: To test the association of the X-chromosome regions (Xp21.1–q21.2 and Xq25–27.2) with Leber hereditary optic neuropathy (LHON) in Chinese patients. METHODS: One hundred and seventy-five male LHON patients with the G11778A mutation and 100 unrelated normal males participated. Twelve microsat...

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Main Authors: Ji, Yanli, Jia, Xiaoyun, Li, Shiqiang, Xiao, Xueshan, Guo, Xiangming, Zhang, Qingjiong
Formato: Artigo
Idioma:Inglês
Publicado em: Molecular Vision 2010
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2838738/
https://ncbi.nlm.nih.gov/pubmed/20300564
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