Leber's hereditary optic neuropathy: the etiological role of a mutation in the mitochondrial cytochrome b gene

Genetics. 1993 Jan;133(1):133-6. doi: 10.1093/genetics/133.1.133.
No abstract available

Publication types

  • Letter
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cytochrome b Group / genetics*
  • Female
  • Humans
  • Male
  • Mitochondria / enzymology*
  • Mutation*
  • Optic Atrophies, Hereditary / genetics*

Substances

  • Cytochrome b Group