Source:http://linkedlifedata.com/resource/lhgdn/association:27779
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
3 putative A1A2 mutations (D718N, R763H, P979L) & 3 that await validation (P796R, E902K, X1021R) were found in familial hemiplegic migraine/and P979L may predispose to seizures and mental retardation/does not play a major role in sporadic HM.
|
| lhgdn:mesh_code |
D008607
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |