C突变的Leber遗传性视神经病变家系的临床特点分析> 2个携带线粒体DNA 14484T>(4)
C突变的Leber遗传性视神经病变家系的临床特点分析'> 2个携带线粒体DNA 14484T>C突变的Leber遗传性视神经病变家系的临床特点分析
[17] Catarino CB，Ahting U，Gusic M，et al. Characterization of a Leber's hereditary optic neuropathy(LHON) family harboring two primary LHON mutations m.11778G>A and m.14484T>C of the mitochondrial DNA[J]. Mitochondrion ......
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