Cite
APA Citation
Veltmann, C., Barajas‐Martinez, H., Wolpert, C., Borggrefe, M., Schimpf, R., Pfeiffer, R., Cáceres, G., Burashnikov, E., Antzelevitch, C., & Hu, D. (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), n/a. http://access.bl.uk/ark:/81055/vdc_100071296416.0x000029