Role of the Pro23Leu mutation in a family affected by retinitis pigmentosa in the Basque Country

Clin Genet. 1999 Nov;56(5):407-8. doi: 10.1034/j.1399-0004.1999.560511.x.
No abstract available

Publication types

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

MeSH terms

  • Aged
  • Humans
  • Male
  • Mutation, Missense
  • Pedigree
  • Polymerase Chain Reaction
  • Retinitis Pigmentosa / genetics*
  • Rhodopsin / genetics*

Substances

  • Rhodopsin