Source:http://linkedlifedata.com/resource/lhgdn/association:47572
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin
|
| lhgdn:mesh_code |
D002313
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |