A Rare Mutation Associated With Probable Late-Onset Leber's Hereditary Optic Neuropathy

J Neuroophthalmol. 2020 Sep;40(3):411-413. doi: 10.1097/WNO.0000000000000962.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • DNA Mutational Analysis
  • DNA, Mitochondrial / genetics*
  • Humans
  • Male
  • Mutation*
  • Optic Atrophy, Hereditary, Leber / genetics*

Substances

  • DNA, Mitochondrial