A sequence polymorphism in the human peripherin/RDS gene

Ítems similars

• Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locus
  per: Kumar-Singh, R., et al.
  Publicat: (1991)
• Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin.
  per: Jordan, S A, et al.
  Publicat: (1992)
• Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse.
  per: Connell, G, et al.
  Publicat: (1991)
• Founder effect, seen in the British population, of the 172 peripherin/RDS mutation-and further refinement of genetic positioning of the peripherin/RDS gene.
  per: Payne, A M, et al.
  Publicat: (1998)
• RDS/peripherin gene mutations are frequent causes of central retinal dystrophies.
  per: Kohl, S, et al.
  Publicat: (1997)