Source:http://linkedlifedata.com/resource/lhgdn/association:12410
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
a mutation in the genomically imprinted potassium channel KCNK9 may have a role in the maternally inherited Birk Barel mental retardation dysmorphism syndrome
|
| lhgdn:mesh_code |
D008607
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |