Tag: Mitochondrial disease

Clinical phenotype and maternal mutation analysis of Leber hereditary optic neuropathy

Authors: Huang Lyuzhen,  Li Tianqi,  Wang Bin,  Li Xiaoxin DOI: 10.3760/cma.j.issn.2095-0160.2016.10.012 Published 2016-10-10 Cite as Chin J Exp Ophthalmol, 2016,34(10): 920-924. Abstract                              [Download PDF] [Read Full Text] Background Leber hereditary optic neuropathy (LHON) is a maternally inherited disease caused by mitochondrial DNA (mtDNA) mutation with the […]