Source:http://linkedlifedata.com/resource/lhgdn/association:40024
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
a distinct SCA (spinocerebellar ataxia) phenotype (SCA27) is associated with a F145S mutation in the fibroblast growth factor 14 (FGF14) gene on chromosome 13q34.
|
| lhgdn:mesh_code |
D020754
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |