Frequency of rare mitochondrial DNA mutations in patients with suspected Leber's hereditary optic neuropathy

J Med Genet. 2003 Jul;40(7):e85. doi: 10.1136/jmg.40.7.e85.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA Mutational Analysis
  • DNA, Mitochondrial / chemistry
  • DNA, Mitochondrial / genetics*
  • Gene Frequency
  • Humans
  • Optic Atrophy, Hereditary, Leber / diagnosis
  • Optic Atrophy, Hereditary, Leber / genetics*
  • Point Mutation

Substances

  • DNA, Mitochondrial

Associated data

  • OMIM/535000