. . . . . . . "[Gain-of-function mutation in KCNQ1, the gene encoding the pore-forming ?-subunit of the IKs channel (KV 7.1), was the first ion channel dysfunction to be associated with familial AF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:14:07+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .