Source:http://linkedlifedata.com/resource/lhgdn/association:28775
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
among 686 autosomal dominant spinocerebellar ataxia families in our cohort, 57 families were identified to have 65 affected individuals, who carried the C-to-T substitution of the puratrophin-1 gene
|
| lhgdn:mesh_code |
D020754
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |