Source:http://linkedlifedata.com/resource/lhgdn/association:4102
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Direct DNA sequencing of the CASR gene in a patient with asymtomatic hypercalcemia heterozygous for c.2501delC, a novel frame shift mutation predicted to cause loss of function of the CASR gene.
|
| lhgdn:mesh_code |
D006934
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |