. . . . . . . . . . . . "[In 2 of 3 families with hereditary short-QT syndrome and a high incidence of ventricular arrhythmias and sudden cardiac death, we identified 2 different missense mutations in the cardiac IKr channel HERG (KCNH2).]. 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 . "2014-10-02T12:33:10+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .