Source:http://linkedlifedata.com/resource/lhgdn/association:36371
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Our results broaden the clinical spectrum associated with POMT2 mutations, which should be considered in patients with CMD associated with microcephaly, and severe mental retardation with or without ocular involvement.
|
| lhgdn:mesh_code |
D008831
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |