Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy

Lancet. 1989 May 13;1(8646):1076-7. doi: 10.1016/s0140-6736(89)92470-7.
No abstract available

Publication types

  • Letter

MeSH terms

  • DNA, Mitochondrial / genetics*
  • Female
  • Hereditary Sensory and Motor Neuropathy / genetics*
  • Humans
  • Mutation*
  • Optic Atrophies, Hereditary / genetics*
  • Polymorphism, Restriction Fragment Length

Substances

  • DNA, Mitochondrial