The use of canine models of inherited retinal degeneration to test novel therapeutic approaches

Author:

Beltran William A.

Publisher

Wiley

Subject

General Veterinary

Reference112 articles.

1. Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene;Suber;Proceedings of the National Academy of Sciences USA,1993

2. Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect;Aguirre;Molecular Vision,1998

3. cGMP phosphodiesterase-alpha mutation causes progressive retinal atrophy in the Cardigan Welsh corgi dog;Petersen-Jones;Investigative Ophthalmology and Visual Science,1999

4. Different RPGR exon ORF15 mutations in Canids provide insights into photoreceptor cell degeneration;Zhang;Human Molecular Genetics,2002

5. Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosa;Kijas;Proceedings of the National Academy of Sciences USA,2002

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