Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic origin

Genomics. 1991 Dec;11(4):1170-1.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Codon
  • Female
  • Genes, Dominant*
  • Humans
  • Ireland
  • Male
  • Mutation*
  • Pedigree
  • Retinitis Pigmentosa / genetics*
  • Rhodopsin / genetics*

Substances

  • Codon
  • Rhodopsin