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Progressive Retinal Atrophy Type 1 (PRA1) – Papillon / Phalène
 Affected Gene: CNGB1
 Inheritance: Autosomal recessive
 Mutation: CanFam3.1 chr2:g.58622673delA; g.586226756insAGCTAC
 OMIA Link: OMIA 002723-9615
 Breed(s) Recommended for Testing: Papillon, Continental Toy Spaniel, Phalène


Symptoms:


     
 
  • Progressive loss of vision
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  • Night blindness (early sign)
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  • Eventual complete blindness
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  • Onset typically occurs in adulthood, but varies by individual
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Reference:
Ahonen SJ, Arumilli M, Lohi H. A CNGB1 frameshift mutation in Papillon and Phalène dogs with progressive retinal atrophy. PLoS One. 2013;8(8):e72122.
PMID: 24015210
DOI: 10.1371/journal.pone.0072122

PRA1 – Progressive Retinal Atrophy Type 1 (Papillon, CNGB1 gene)

C$65.00Price

5 tests et + 55$ch.

Quantity

After your samples are received at the laboratory, please allow 10 to 15 business days for your results to be sent.

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