Source:http://linkedlifedata.com/resource/lhgdn/association:53402
Predicate | Object |
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lhgdn:found_in | |
lhgdn:geneRifSource |
Here we report the first pediatric case of restrictive cardiomyopathy secondary to a de novo mutation in the cardiac myosin heavy chain gene MYH7.
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lhgdn:mesh_code |
D002313
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lhgdn:associationIdType | |
lhgdn:umls_code |