Source:http://linkedlifedata.com/resource/lhgdn/association:10052
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Describe a novel dominant pathogenic GJB2 mutation in a family affected with bilateral mild/moderate high-frequency hereditary non-syndromic sensorineural hearing loss.
|
| lhgdn:mesh_code |
D006319
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |