Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy

Am J Hum Genet. 1994 Nov;55(5):1063-6.
No abstract available

Publication types

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

MeSH terms

  • Belgium
  • DNA Probes
  • DNA, Mitochondrial / genetics*
  • Female
  • Germany
  • Humans
  • Male
  • Mutation*
  • Optic Atrophies, Hereditary / genetics*
  • Pedigree

Substances

  • DNA Probes
  • DNA, Mitochondrial