Source:http://linkedlifedata.com/resource/lhgdn/association:29775
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Frataxin and cardiac troponin T gene mutations co-exist in a child with Friedreich ataxia and familial hypertrophic cardiomyopathy.
|
| lhgdn:mesh_code |
D005621
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |