Publication | Open Access

Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy

Mendelian DisorderOphthalmologyGenetic DisorderGeneticsHuman PolymorphismMolecular BiologyLeber Hereditary Optic NeuropathyMolecular GeneticsDisease Gene IdentificationAsian-specific Mtdna BackgroundsPrimary G11778a MutationNeuropathologyMedicineHereditary Optic NeuropathyNeurogenetics