. . . . . . . "[study identified T to A transition mutation at position 4, 603 in exon 40 resulting in substitution of arginine for tryptophan at amino acid residue 1, 535 in regulatory domain of ankyrin-B; this novel mutation may be a cause of type 4 long QT syndrome]. 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 . "2017-10-17T13:10:28+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .