Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa

Nat Genet. 1999 Dec;23(4):393-4. doi: 10.1038/70496.
No abstract available

Publication types

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

MeSH terms

  • Aged
  • Eye Proteins / genetics*
  • Female
  • Heterozygote
  • Homozygote
  • Humans
  • Male
  • Mutation*
  • Pedigree
  • Receptors, Cell Surface / genetics*
  • Receptors, G-Protein-Coupled*
  • Retinitis Pigmentosa / genetics*
  • Retinitis Pigmentosa / pathology
  • Rod Opsins / genetics

Substances

  • Eye Proteins
  • G protein-coupled receptor RGR
  • Receptors, Cell Surface
  • Receptors, G-Protein-Coupled
  • Rod Opsins