Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy

Am J Hum Genet. 1996 Jul;59(1):248-52.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Africa
  • DNA, Mitochondrial / genetics*
  • Evolution, Molecular
  • Female
  • Haplotypes
  • Humans
  • Male
  • Mutation
  • Optic Atrophies, Hereditary / genetics*

Substances

  • DNA, Mitochondrial