Nat. Genet. 45, 1044–1049 (2013); published online 21 July 2013; corrected after print 4 October 2013
In the version of this article initially published, Martin Borggrefe and Rainer Schimpf were inadvertently omitted from the author list. Both are affiliated with the First Department of Medicine (Cardiology), University Medical Center, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany, and with DZHK (German Centre for Cardiovascular Research), partner site Heidelberg/Mannheim, Mannheim, Germany. In addition, one of the study's funding sources (the Ministry of Health, Labour and Welfare of Japan, research grant for cardiovascular diseases, H24-033) was omitted from the Acknowledgments section. These errors have been corrected in the HTML and PDF versions of the article.
Additional information
The online version of the original article can be found at 10.1038/ng.2712
Rights and permissions
About this article
Cite this article
Bezzina, C., Barc, J., Mizusawa, Y. et al. Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Nat Genet 45, 1409 (2013). https://doi.org/10.1038/ng1113-1409b
Published:
Issue Date:
DOI: https://doi.org/10.1038/ng1113-1409b
