The impact of common and rare genetic variants on bradyarrhythmia development
Lu-Chen C Weng, Joel T Rämö, Sean J. Jurgens, Shaan Khurshid et autres
To broaden our understanding of bradyarrhythmias and conduction disease, we performed common variant genome-wide association analyses in up to 1.3 million individuals and rare variant burden testing in 460,000 individuals for sinus node dysfunction (SND), distal conduction disease (DCD) and pacemaker (PM) …
us, fi, nl, se, ca, dk (code pays fourni par la source)
23 citations
Nature Genetics