Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families

Authors:	Liu Xiao-Ling Zhou Xiangtian Zhou Jian Zhao Fuxin Zhang Juanjuan Li Chengwu Ji Yanchun Zhang Yu Wei Qi-Ping Sun Yan-Hong Yang Li Lin Bing Yuan Yumin Li Yingzi Qu Jia Guan Min-Xin

Affiliation:	¹ School of Ophthalmology and Optometry, Wenzhou Medical College, Wenzhou, Zhejiang, China ² Attardi Institute of Mitochondrial Biomedicine and Zhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical College, Wenzhou, Zhejiang, China ³ Department of Ophthalmology, Beijing University of Chinese Medicine and Pharmacology, Beijing, China ⁴ Eye Hospital, Chinese Academy of China Medical Sciences, Beijing, China ⁵ Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio ⁶ Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio

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