Leber's hereditary optic neuropathy (LHON)-associated ND5 12338T > C mutation altered the assembly and function of complex I, apoptosis and mitophagy

Leber 遗传性视神经病变 (LHON) 相关 ND5 12338T > C 突变改变了复合物 I 的组装和功能、细胞凋亡和线粒体自噬