[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.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE