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Progressive Retinaatrophie, Late Onset (PRA-IFT122) Searchterm 0 delivers comprehensive genetic insights

SKU: 69707917410
4.5

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0 delivers comprehensive genetic insights – supporting informed decisions in health

Die Symptome umfassen Hepatomegalie

The disease is a part of a group of ciliopathies presenting as inherited hepatorenal fibrocystic disorders

it also stabilizes blood coagulation factor VIII (FVIII)

das in vielen verschiedenen Hunderassen bekannt ist

Progressive Retinaatrophie, Late Onset (PRA-IFT122) Searchterm 0 delivers comprehensive genetic insightsProgressive retinal atrophy (PRA) is a group of hereditary diseases characterized by vision impairment due to retinal degeneration, which is a result of progressive cell death of the rod and cone photoreceptors in the retina. A late onset variant of PRA called IFT122 was characterized in Lapponian herders. Clinical symptoms, which include retinal thinning, atrophy of the optic disc, diffuse tapetal hyperreflectivity, retinal vascular weakening, night

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