Ocular signs associated with a rhodopsin mutation (Cys-167-->Arg) in a family with autosomal dominant retinitis pigmentosa

Br J Ophthalmol. 1998 Jun;82(6):709. doi: 10.1136/bjo.82.6.709.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Child
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Pedigree
  • Phenotype
  • Retinitis Pigmentosa / genetics*
  • Rhodopsin / genetics*

Substances

  • Rhodopsin

Grants and funding