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-Zitierstil (17. Ausg.)Veltmann, Christian, Martin Borggrefe, und 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-Zitierstil (9. Ausg.)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.