Cite
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
MLA
Bezzina, Connie R., et al. “Common Variants at SCN5A-SCN10A and HEY2 Are Associated with Brugada Syndrome, a Rare Disease with High Risk of Sudden Cardiac Death.” Nature Genetics, vol. 45, no. 9, Sept. 2013, pp. 1044–49. EBSCOhost, https://doi.org/10.1038/ng.2712.
APA
Bezzina, C. R., Barc, J., Mizusawa, Y., Remme, C. A., Gourraud, J.-B., Simonet, F., Verkerk, A. O., Schwartz, P. J., Crotti, L., Dagradi, F., Guicheney, P., Fressart, V., Leenhardt, A., Antzelevitch, C., Bartkowiak, S., Borggrefe, M., Schimpf, R., Schulze-Bahr, E., Zumhagen, S., … Redon, R. (2013). Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Nature Genetics, 45(9), 1044–1049. https://doi.org/10.1038/ng.2712
Chicago
Bezzina, Connie R, Julien Barc, Yuka Mizusawa, Carol Ann Remme, Jean-Baptiste Gourraud, Floriane Simonet, Arie O Verkerk, et al. 2013. “Common Variants at SCN5A-SCN10A and HEY2 Are Associated with Brugada Syndrome, a Rare Disease with High Risk of Sudden Cardiac Death.” Nature Genetics 45 (9): 1044–49. doi:10.1038/ng.2712.