Progressive Retinaatrophie (rcd1a-PRA)

(Sloughi)plus
Disease
autosomal recessive
Heredity
In the Sloughi breed, dysplasia of cones and rods occurs (a so-called rod cone dysplasia type 1 (rcd1)). The rcd mutation is characterised by an early onset of the disease.
Test duration
sequencing
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