Eyes genetic problems: CSNB (Congenital Stationary Night Blindness) and PRA (Progressing Retinal Atrophy)

the laboratory for genetic analysis:
OptiGen, USA
VHL, Netherlands
Antagene, France (by post)
Genomia, Czech Republik (csnb by post)
Dajbych, Slovakia (pra by post)
Finnzymes, Finland - Espoo
Genecontrol, Germany (csnb)
Healthgene, Canada (csnb)

Congenital Stationary Night Blindness (CSNB), Test for briards (Optigen site)
Congenital stationary night blindness in the dog: common mutation in the RPE65 gene indicates founder effect, "Molecular Vision" 1998; 4:23.
Progressive retinal degeneration (PRD) or progressive retinal atrophy (PRA) - site Animal Eye Specialists
Retinal dysplasia (RD) and retinal folds - site Animal Eye Specialists
Canine Eye Registration Foundation (CERF) - USA
The European College of Veterinary Ophthalmologists (ECVO)
Journal of Veterinary Ophthalmology
International Society of Veterinary Ophthalmology Newsletters
"When Good Dogs Get Bad Genes" (PRCD-PRA)
Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse - "Genetics", 2008 August; 179(4): 1861-1870.

LCA - Lebers congenital amaurosis
Success in sight: The eyes have it! Ocular gene therapy trials for LCA look promising - Gene Therapy No 15 (2008)
Researchers bring sight to the blind - Lebers congenital amaurosis (LCA) (Filadelfia Univ., USA, 28.04.08)
Project 3000 - Two Major Sports Figures Team Up to Fight an Important Cause of Childhood Blindness
Leber congenital amaurosis, "Genetics Home Reference", aug 2010 (also catalogue of links)