Source:http://linkedlifedata.com/resource/lhgdn/association:47309
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
No large deletions at the SCN1A locus were found in any of the patients/different point mutations were identified in 12 patients: 10 with SMEI, 1 with generalized epilepsy with febrile seizures plus, and 1 with cryptogenic focal epilepsy.
|
| lhgdn:mesh_code |
D003294
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |