Preferential rod and cone photoreceptor abnormalities in heterozygotes with point mutations in the RDS gene

Exp Eye Res. 1996 Nov;63(5):603-8. doi: 10.1006/exer.1996.0152.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Eye Proteins / genetics*
  • Heterozygote
  • Humans
  • Intermediate Filament Proteins / genetics*
  • Membrane Glycoproteins*
  • Middle Aged
  • Nerve Tissue Proteins*
  • Peripherins
  • Photoreceptor Cells / physiopathology*
  • Point Mutation*
  • Retinal Degeneration / genetics*

Substances

  • Eye Proteins
  • Intermediate Filament Proteins
  • Membrane Glycoproteins
  • Nerve Tissue Proteins
  • PRPH2 protein, human
  • Peripherins