Source:http://linkedlifedata.com/resource/lhgdn/association:63014
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
In Kallmann syndrome patients, ten different missense mutations have been identified in PROKR2.
|
| lhgdn:mesh_code |
D017436
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |