Low frequency of rhodopsin mutations in South African patients with autosomal dominant retinitis pigmentosa

Clin Genet. 2000 Jul;58(1):77-8. doi: 10.1034/j.1399-0004.2000.580114.x.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Codon
  • DNA Mutational Analysis
  • Genes, Dominant
  • Humans
  • Mutation
  • Polymorphism, Single-Stranded Conformational
  • Retinitis Pigmentosa / genetics*
  • Rhodopsin / genetics*
  • South Africa

Substances

  • Codon
  • Rhodopsin