
Characterization of a Leber's hereditary optic neuropathy (LHON) family harboring two primary LHON mutations m.11778GÂ >Â A and m.14484TÂ >Â C of the mitochondrial DNA
Keywords: زنجیر تنفسی; LHON; Mitochondriopathy; Mitochondrial DNA; Complex I; Respiratory chain; Oxidative phosphorylation;