Source:http://linkedlifedata.com/resource/lhgdn/association:28124
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
study highlights the role of LMNA mutations in dilated cardiomyopathy and related disorders/severe phenotype in p.N195K mutation carriers and preferential cardiac conduction disease in p.R225X carriers was encountered.
|
| lhgdn:mesh_code |
D002311
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |