Related Articles
Mitochondrial tRNAAla 5601C>T variant may affect the clinical expression of the LHON‑related ND4 11778G>A mutation in a family
Leber's hereditary optic neuropathy is potentially associated with a novel m.5587T>C mutation in two pedigrees
Two families with Leber's hereditary optic neuropathy carrying G11778A and T14502C mutations with haplogroup H2a2a1 in mitochondrial DNA
Characterization of retinal nerve fiber layer thickness changes associated with Leber's hereditary optic neuropathy by optical coherence tomography
Clinical characteristics of nonglaucomatous optic disc cupping