Source:http://linkedlifedata.com/resource/lhgdn/association:9240
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Several oculomotor deficits of spinocerebellar ataxia type 17 (SCA17) mutation carriers are compatible with cerebellar degeneration.
|
| lhgdn:mesh_code |
D020754
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |