APA (7th ed.) Citation

Veltmann, C., Borggrefe, M., & Schimpf, R. (2016). Further insights in the most common SCN5A mutation causing overlapping phenotype of long QT syndrome, brugada syndrome, and conduction defect. Journal of the American Heart Association, 5(7), . https://doi.org/10.1161/JAHA.116.003379

Chicago Style (17th ed.) Citation

Veltmann, Christian, Martin Borggrefe, and Rainer Schimpf. "Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect." Journal of the American Heart Association 5, no. 7 (2016). https://doi.org/10.1161/JAHA.116.003379.

MLA (9th ed.) Citation

Veltmann, Christian, et al. "Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect." Journal of the American Heart Association, vol. 5, no. 7, 2016, https://doi.org/10.1161/JAHA.116.003379.