. . . . . . . . . . . . "[Rare mutations in KCNH2 provide the pathogenic substrate for type 2 congenital long QT syndrome (LQTS), thus placing this cardiac potassium channel squarely in the intersection between congenital LQTS (the Rosetta stone of the heritable channelopathies) and acquired LQTS (drug-induced TdP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2016-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2016-05-13T12:45:40+02:00"^^ . . . . . . . . . . . "v4.0.0.0" . "v4.0.0" .