线粒体T12338C突变可能是与Leber遗传性视神经病变相关的突变位点
冀延春，刘晓玲，赵福新，张娟娟，章豫，周翔天，瞿佳，管敏鑫
The mitochondrial ND5 T12338C mutation may be associated with Leber’s hereditary optic neuropathy in two Chinese families
JI Yan-Chun, LIU Xiao-Ling, ZHAO Fu-Xin, ZHANG Juan-Juan, ZHANG Yu, ZHOU Xiang-Tian, QU Jia, GUAN Min-Xin
遗传
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2011, (4): 322
-328
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DOI: 10.3724/SP.J.1005.2011.00322
