Source:http://linkedlifedata.com/resource/lhgdn/association:62256
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
We have identified a novel missense mutation (C722G) in the CHRM2 gene associated with familial dilated cardiomyopathy, which correlates with autoantibodies against CHRM2/with C722G mutation have more progressive disease
|
| lhgdn:mesh_code |
D002311
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |