Source:http://linkedlifedata.com/resource/lhgdn/association:60850
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Heterozygous deletion of the 5?part of the ITPR1 gene, encompassing exons 1-10, 1-40, and 1-44 in three studied families, underlies spinocerebellar ataxia 15 in humans.
|
| lhgdn:mesh_code |
D020754
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |