Source:http://linkedlifedata.com/resource/lhgdn/association:29434
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Mutation analysis in 12 unrelated patients with Usher syndrome, each with one mutation in exons 1-21, revealed three different truncating mutations in four patients and two missense mutations in one patient
|
| lhgdn:mesh_code |
D052245
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |