Source:http://linkedlifedata.com/resource/lhgdn/association:29435
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
investigation of 9 Usher syndrome type 2 families from Quebec & New Brunswick; seven USH2A mutations were identified in eight patients; one of them, c.4338 _ 4339delCT, accounts for 10 out of 18 disease alleles
|
| lhgdn:mesh_code |
D052245
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |