. . . . . . . . . . . . "[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 . . . . . "2014-02-25"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2014-10-02T12:40:58+02:00"^^ . . . . . . . . . . . "v2.1.0.0" . "v2.1.0" .