Source:http://linkedlifedata.com/resource/lhgdn/association:12129
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease
|
| lhgdn:mesh_code |
D009136
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |