Source:http://linkedlifedata.com/resource/lhgdn/association:29306
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
analysis of a novel genetic subtype for Usher syndrome, USH2D, which is caused by mutations in whirlin
|
| lhgdn:mesh_code |
D052245
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |