Publication | Closed Access

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

BiologyMendelian DisorderGenetic DisorderNatural SciencesGeneticsMolecular BiologyLeber Hereditary Optic NeuropathyPrimary Lhon MutationsMolecular GeneticsDisease Gene IdentificationMedicineHereditary Optic NeuropathyMitochondrial DnaNeurogenetics