[Understanding the structural and functional role of cardiac myosin-binding protein C in the heart is clinically relevant, as cMyBP-C gene mutations are a widely recognized cause of familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE