Combination Labradoodle

LABOKLIN Service ID: 8743

The following tests are included in this combination:

Centronuclear myopathy (CNM), Degenerative myelopathy (exon 2), Exercise induced collapse (EIC), Hereditary nasal parakeratosis (HNPK), Neonatal encephalopathy with seizures (NEWS), Skeletal dysplasia 2 (SD2), von Willebrand disease type I (vWD 1), Progressive retinal atrophy* (prcd-PRA) and Progressive retinal atrophy (rcd4-PRA)

Breed list	Labradoodle
Heredity	Further information could be found in the description of the corresponding genetic test.
Duration	1 - 2 weeks after arrival of the sample in the lab