Progressive retinal atrophy (CNGB1: c.2685delA2687_2688insTAGCTA p.Tyr889Serfs*5)
Progressive retinal atrophy (PRA1) is a genetic disease characterised by the degeneration of rod photoreceptors in the eye. The first symptoms of vision loss appear between the ages of 4 and 6.
Transmission
Autosomal recessiveBreed
Papillon, Phalène



