Eyes
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Cone-rod dystrophy 4 - Progressive Retinal...
Order number: GSD361
€53.90 VAT incl.
List price - personal prices are available after logging into ATC user account.
List price - personal prices are available after logging into ATC user account.
Application:
- Identification of heterozygous carriers
The test examines the mutation in the RPGRIP1 gene, which is a risk factor for cone-rod dystrophy 4-progressive retinal atrophy (crd4/cord1-PRA) in longhaired miniature dachshunds.This is a complex disease in which other gene mutations also play an important role in disease progression.
- Identification of heterozygous carriers
The test examines the mutation in the RPGRIP1 gene, which is a risk factor for cone-rod dystrophy 4-progressive retinal atrophy (crd4/cord1-PRA) in longhaired miniature dachshunds.This is a complex disease in which other gene mutations also play an important role in disease progression.
crd-PRA
Order number: GSD307
€53.90 VAT incl.
List price - personal prices are available after logging into ATC user account.
List price - personal prices are available after logging into ATC user account.
Test indication: a) Identfication of carriers among offsping of a carrier x free mating. b) Differential diagnosis of clinical PRA cases.
crd-PRA is an early onset type of PRA described for wirehaired dachshunds. The defect occurs in the NPHP4 gene and has an autosomal-recessive mode of inheritance.
crd-PRA is an early onset type of PRA described for wirehaired dachshunds. The defect occurs in the NPHP4 gene and has an autosomal-recessive mode of inheritance.
Golden Retriever PRA 1
Order number: GSD514
€53.90 VAT incl.
List price - personal prices are available after logging into ATC user account.
List price - personal prices are available after logging into ATC user account.
Application: - Carrier identification - Differential diagnosis in clinical PRA.
With this test we investigate if the dog carries a mutation in the SLC4A3-gene that was identified as the cause of GR_PRA1. PRA (Progressive Retinal Atrophy) is the name for a group of diseases of the eye. They are characterised by a progressive degeneration of the retina that eventually leads...
With this test we investigate if the dog carries a mutation in the SLC4A3-gene that was identified as the cause of GR_PRA1. PRA (Progressive Retinal Atrophy) is the name for a group of diseases of the eye. They are characterised by a progressive degeneration of the retina that eventually leads...
Golden Retriever PRA 2
Order number: GSD515
€53.90 VAT incl.
List price - personal prices are available after logging into ATC user account.
List price - personal prices are available after logging into ATC user account.
Application: - Carrier identification - Differential diagnosis in clinical PRA.
With this test we investigate if the dog carries a mutation in the TTC8-gene that was identified as the cause of GR_PRA2. PRA (Progressive Retinal Atrophy) is the name for a group of diseases of the eye. They are characterised by a progressive degeneration of the retina that eventually leads to...
With this test we investigate if the dog carries a mutation in the TTC8-gene that was identified as the cause of GR_PRA2. PRA (Progressive Retinal Atrophy) is the name for a group of diseases of the eye. They are characterised by a progressive degeneration of the retina that eventually leads to...
STGD - Stargardt Disease
Order number: GSD573
€53.90 VAT incl.
List price - personal prices are available after logging into ATC user account.
List price - personal prices are available after logging into ATC user account.
Application:
- Identification of heterozygous carriers for breeding selection
- Differential diagnosis in case of visual impairment
The test examines whether the mutation (c.4176insC) in the ABCA4 gene that causes 'Stargardt Disease' (STGD) is present. The mode of inheritance is autosomal recessive, so that only animals in which both hereditary factors are defective develop...
- Identification of heterozygous carriers for breeding selection
- Differential diagnosis in case of visual impairment
The test examines whether the mutation (c.4176insC) in the ABCA4 gene that causes 'Stargardt Disease' (STGD) is present. The mode of inheritance is autosomal recessive, so that only animals in which both hereditary factors are defective develop...