The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases.

MLA

Winkel, Bo Gregers, et al. “The Prevalence of Mutations in KCNQ1, KCNH2, and SCN5A in an Unselected National Cohort of Young Sudden Unexplained Death Cases.” Journal of Cardiovascular Electrophysiology, vol. 23, no. 10, Oct. 2012, pp. 1092–98. EBSCOhost, https://doi.org/10.1111/j.1540-8167.2012.02371.x.

APA

Winkel, B. G., Larsen, M. K., Berge, K. E., Leren, T. P., Nissen, P. H., Olesen, M. S., Hollegaard, M. V., Jespersen, T., Yuan, L., Nielsen, N., Haunsø, S., Svendsen, J. H., Wang, Y., Kristensen, I. B., Jensen, H. K., Tfelt-Hansen, J., & Banner, J. (2012). The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases. Journal of Cardiovascular Electrophysiology, 23(10), 1092–1098. https://doi.org/10.1111/j.1540-8167.2012.02371.x

Chicago

Winkel, Bo Gregers, Maiken Kudahl Larsen, Knut Erik Berge, Trond Paul Leren, Peter Henrik Nissen, Morten Salling Olesen, Mads Vilhelm Hollegaard, et al. 2012. “The Prevalence of Mutations in KCNQ1, KCNH2, and SCN5A in an Unselected National Cohort of Young Sudden Unexplained Death Cases.” Journal of Cardiovascular Electrophysiology 23 (10): 1092–98. doi:10.1111/j.1540-8167.2012.02371.x.