摘要 : The ND4 G11778A mutation is the most common mitochondrial DNA mutation leading to Leber's hereditary optic neuropathy (LHON). Despite considerable clinical evidences, the modifier role of nuclear background and mitochondrial haplo... 展开
作者 | Guan MX Zhou X Liang M Qu J Qian Y |
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作者单位 | |
期刊名称 | 《Mitochondrion》 |
总页数 | 7 |
语种/中图分类号 | 英语 / Q93 |
关键词 | Penetrance Leber's optic neuropathy Mitochondrion Complex III Complex I Mutaion Chinese |
馆藏号 | N2008EPST0011265 |