A new mitochondrial DNA mutation in the tRNA leucine 1 gene (C3275A) in a patient with Leber's hereditary optic neuropathy

Hum Mutat. 2000 Jan;15(1):120-1. doi: 10.1002/(SICI)1098-1004(200001)15:1<120::AID-HUMU33>3.0.CO;2-8.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosomes, Human, Pair 12
  • DNA, Mitochondrial / genetics*
  • Humans
  • Molecular Sequence Data
  • Optic Atrophies, Hereditary / genetics*
  • Point Mutation
  • Polymerase Chain Reaction
  • RNA, Transfer, Amino Acyl / genetics*

Substances

  • DNA, Mitochondrial
  • RNA, Transfer, Amino Acyl

Associated data

  • GENBANK/J01415