Source:http://linkedlifedata.com/resource/lhgdn/association:29745
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Two novel mutations in OA1 gene were identified in two families with ocular albinism/mutations are likely loss-of-function mutations/in OA1 gene are associated with majority of X-linked ocular albinism cases.
|
| lhgdn:mesh_code |
D016117
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |