From genotype to phenotype in Leber hereditary optic neuropathy: still more questions than answers

J Neuroophthalmol. 2002 Dec;22(4):257-61. doi: 10.1097/00041327-200212000-00001.
No abstract available

Publication types

  • Comment
  • Editorial
  • Review

MeSH terms

  • Animals
  • DNA, Mitochondrial / genetics
  • Genotype
  • Humans
  • Mice
  • Optic Atrophy, Hereditary, Leber / genetics*
  • Phenotype
  • Point Mutation / physiology

Substances

  • DNA, Mitochondrial