Source:http://linkedlifedata.com/resource/lhgdn/association:28950
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
This study describes a mutation in OPA1 causing a unique syndrome of optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia.
|
| lhgdn:mesh_code |
D006319
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |