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| Mitochondrial variants may influence the phenotypic manifestation of Leber＇ s hereditary optic neuropathy-associated ND4 G 11778A mutation | |
| 作者单位： | [1]Zhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Wenzhou Medical College, Wenzhou 325035, China [2]School of Ophthalmology and Optometry, Wenzhou Medical College, Wenzhou 325003, China [3]The Third Affiliated Hospital, Xinxiang Medical College, Xinxiang 453003, China [4]The FirstAffiliated Hospital, Fujian Medical University, Fuzhou 350005, China [5]Division of Human Genetics, Cincinnati Children＇s Hospital Medical Center, Cincinnati, Ohio 45229, USA |
| 摘 要： | |
| 关 键 词： | 线粒体 基因 伯氏遗传性视神经 病变 |
| 本文献已被 维普 等数据库收录！ | |