Identical mutation in a novel retinal gene causes progressive rod–cone degeneration in dogs and retinitis pigmentosa in humans

Author:

Zangerl Barbara,Goldstein Orly,Philp Alisdair R.,Lindauer Sarah J.P.,Pearce-Kelling Susan E.,Mullins Robert F.,Graphodatsky Alexander S.,Ripoll Daniel,Felix Jeanette S.,Stone Edwin M.,Acland Gregory M.,Aguirre Gustavo D.

Publisher

Elsevier BV

Subject

Genetics

Reference35 articles.

1. Pathogenesis of progressive rod–cone degeneration in miniature poodles;Aguirre;Invest. Ophthalmol. Visual Sci.,1982

2. Models, mutants and man: searching for unique phenotypes and genes in the dog model of inherited retinal degeneration;Aguirre,2006

3. Interphotoreceptor retinoid-binding protein (IRBP) in progressive rod–cone degeneration (prcd)—Biochemical, immunocytochemical and immunologic studies;Wiggert;Exp. Eye Res.,1991

4. Plasma lipid changes in PRCD-affected and normal miniature poodles given oral supplements of linseed oil: indications for the involvement of n-3 fatty acids in inherited retinal degenerations;Anderson;Exp. Eye Res.,1994

5. Structural changes of the interphotoreceptor matrix in an inherited retinal degeneration: a lectin cytochemical study of progressive rod–cone degeneration;Mieziewska;Invest. Ophthalmol. Visual Sci.,1993

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