CASR single gene test
- Plus Analysis (Sequence + Del/Dup (CNV))
Test code: S00298
- Neonatal hyperparathyroidism
- Familial Hypocalciuric hypercalcemia with transient Neonatal hyperparathyroidism
Alternative gene name
FHH, NSHPT, GPRC2A
Panels that include the gene
- Comprehensive Skeletal Dysplasias and Disorders Panel
- Comprehensive Epilepsy Panel
- Beyond Paediatric Epilepsy panel
- Skeletal Dysplasia with Abnormal Mineralization Panel
- Idiopathic Generalized and Focal Epilepsy Panel
- Comprehensive Skeletal / Malformation Syndrome Panel
- Hyperparathyroidism Panel
- Bartter Syndrome Panel
For pricing inquiries, please contact (firstname.lastname@example.org) or call the sales support team +358 40 2511 372.
Accepted sample types
- EDTA blood, min. 1 ml
- Purified DNA, min. 5μg
- Saliva (Oragene DNA OG-500 kit)
Label the sample tube with your patient’s name, date of birth and the date of sample collection.
Note that we do not accept DNA samples isolated from formalin-fixed paraffin-embedded (FFPE) tissue.