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High prevalence of genetic variants previously associated with LQT syndrome in new exome data
Refsgaard, Lena, Holst, Anders G, Sadjadieh, Golnaz, Haunsø, Stig, Nielsen, Jonas B, Olesen, Morten SVolume:
20
Language:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2012.23
Date:
August, 2012
File:
PDF, 205 KB
english, 2012