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    Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families

    Leber's hereditary optic neuropathy (LHON) is characterized by maternally transmitted, bilateral, central vision loss in young adults. It is caused by mutations in the mitochondrial DNA (mtDNA) encoded genes ...

    Michael D. Brown, Sergei Zhadanov, Jon C. Allen, Seyed Hosseini in Human Genetics (2001)