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Progressive Retinaatrophie, Rod-cone Dysplasie 4 (PRA-rcd4) ISAG Mutation: MTM1 gene

SKU: 46011315090
4.8

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Description

Mutation: MTM1 gene

die bei Scottish Deerhounds beschrieben wurde

Mutation: ADAMTS17 gene

in French Bulldog L1 and L4 mutations can cause long coat

predominance of type I fibres

Progressive Retinaatrophie, Rod-cone Dysplasie 4 (PRA-rcd4) ISAG Mutation: MTM1 geneProgressive retinal atrophy (PRA) is an inherited disease that occurs in many breeds of dogs and is reflected in various clinically indistinguishable forms. Progressive rod and cone degeneration in retina leads to progressive vision loss, which ends with total blindness. RCD4 is a form of PRA that was first described in Gordon Setters and later found in several other dog breeds. Gradual photoreceptor cell degeneration is typical for this form of the

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