Source:http://linkedlifedata.com/resource/lhgdn/association:46849
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
The SCN5A (W1191X) mutation is associated with Brugada syndrome and resulted in the loss of function of the cardiac sodium channel.
|
| lhgdn:mesh_code |
D053840
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |