Source:http://linkedlifedata.com/resource/lhgdn/association:47526
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
infantile case of restrictive cardiomyopathy caused by a de novo mutation of the cardiac troponin T gene.
|
| lhgdn:mesh_code |
D002313
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |