. . . . . . . "[results suggest that T322M is a novel mutation that caused Romano-Ward syndrome with high intrafamilial variability in the heterozygous carriers and typical Jervell and Lange-Nielsen syndrome in the homozygous carriers within this Chinese family]. 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 . "2017-10-17T13:14:06+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .