Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy

Am J Hum Genet. 1996 Aug;59(2):481-5.
No abstract available

Publication types

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

MeSH terms

  • Australia / epidemiology
  • DNA, Mitochondrial*
  • Europe / epidemiology
  • Female
  • Humans
  • Male
  • Models, Genetic
  • Mutation*
  • New Zealand / epidemiology
  • Optic Atrophies, Hereditary / classification
  • Optic Atrophies, Hereditary / epidemiology
  • Optic Atrophies, Hereditary / genetics*
  • Optic Atrophies, Hereditary / pathology
  • Pedigree

Substances

  • DNA, Mitochondrial