Disease relevance of the so-called secondary Leber hereditary optic neuropathy mutations

Am J Hum Genet. 1997 Jun;60(6):1539-42. doi: 10.1016/S0002-9297(07)64248-7.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Australia
  • Europe
  • Family
  • Female
  • Germany
  • Humans
  • Male
  • Mutation*
  • New Zealand
  • Optic Atrophies, Hereditary / genetics*
  • Pedigree
  • Reference Values
  • White People