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.
Catarino CB1, Ahting U2, Gusic M3, Iuso A3, Repp B3, Peters K4, Biskup S4, von Livonius B5, Prokisch […]