Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death
Tom Rossenbacker, Sheila J. Carroll, Huajun Liu, Cuno Kuipéri, Thomy de Ravel, Koenraad Devriendt, Peter Carmeliet, Robert S. Kass, Hein Heidbüchel (2004). Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death. , 1(5), DOI: https://doi.org/10.1016/j.hrthm.2004.07.001.
