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 |