Combination hereditary diseases cat

LABOKLIN Service ID: 8350

The comnination includes the following tests:
HCM1 (Hypertrophc cardiomyopathy), HCM3 (Hypertrophc cardiomyopathy), GSD IV (Glycogen storage disease Type IV), PKD (Polycystic kidney disease), PK-Def. (Pyruvat kinase deficiency), rdAc-PRA (Progressive retinal atrophy), SMA (Spinal muscular atrophy), genetic blood group testing

Method	TaqMan SNP assay, FLP
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