Source:http://linkedlifedata.com/resource/lhgdn/association:62734
Predicate | Object |
---|---|
lhgdn:found_in | |
lhgdn:geneRifSource |
Centrosome malfunction due to the CDK5RAP2 mutations may underlie autosomal recessive primary microcephaly.
|
lhgdn:mesh_code |
D008831
|
lhgdn:associationIdType | |
lhgdn:umls_code |