Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa

Hum Mol Genet. 1994 Jul;3(7):1203. doi: 10.1093/hmg/3.7.1203.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Codon / genetics
  • Genes
  • Genes, Dominant
  • Humans
  • Molecular Sequence Data
  • Point Mutation*
  • Retinitis Pigmentosa / classification
  • Retinitis Pigmentosa / genetics*
  • Rhodopsin / genetics*

Substances

  • Codon
  • Rhodopsin