57,48 47,50 excl. VAT

P311

Congenital stationary night blindness is characterised by difficulties in adapting to low light situations.

10 working days

Specifications

Breeds

, , , , , , ,

Gene

Organ

specimen

Hair, Blood EDTA, Blood Heparin, Semen, Tissue

Mode of Inheritance

Chromosome

Also known as

Year Published

General information

Congenital stationary night blindness is characterised by difficulties in adapting to low light situations. The disease is present from birth onwards and is non-progressive.

Clinical features

The disease is associated with short-sightedness and (in case homozygous for LP) Leopard complex spotting.

Additional information

References

Pubmed ID: 24167615

Omia ID: 1341

How does it work?

Learn more

1. Select your product(s)

Select your single test, a CombiBreed Package or create your own Bundle.

2. Collect DNA sample

Collect DNA material as indicated with our products and send it to our laboratory.

3. Results

We handle your DNA sample with care and provide you with the results.

Related products