Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings

Am J Hum Genet. 1995 Oct;57(4):954-7.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • DNA, Mitochondrial / analysis*
  • Humans
  • Middle Aged
  • Optic Atrophies, Hereditary / genetics*
  • Point Mutation*

Substances

  • DNA, Mitochondrial