Source:http://linkedlifedata.com/resource/lhgdn/association:18274
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
These data are consistent with the notion that a R44H missense mutation in human RGS2 produces a hypomorphic allele that may lead to altered receptor-mediated G (q) inhibition and contribute to the development of hypertension in affected subjects.
|
| lhgdn:mesh_code |
D006973
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |