Source:http://linkedlifedata.com/resource/lhgdn/association:58623
Predicate | Object |
---|---|
lhgdn:found_in | |
lhgdn:geneRifSource |
mutations in KCND2 and KCND3 are not a frequent cause of long QT syndrome
|
lhgdn:mesh_code |
D008133
|
lhgdn:associationIdType | |
lhgdn:umls_code |