. . . . . . . "[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]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:11:33+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .