Cite
MLA Citation
Christian Veltmann 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, p. n/a. http://access.bl.uk/ark:/81055/vdc_100071296416.0x000029