Source:http://linkedlifedata.com/resource/lhgdn/association:36516
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Identification of SIX1 mutations as causing branchio-oto-renal syndrome offers insights into the molecular basis of otic and renal developmental diseases in humans
|
| lhgdn:mesh_code |
D019280
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |