Source:http://linkedlifedata.com/resource/lhgdn/association:47303
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
This suggests that mutations in the SCN1B gene is not a prevalent cause of familial cases of FS and epilepsy or GEFS+ in Scandinavia.
|
| lhgdn:mesh_code |
D004827
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |