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

doi:10.1016/j.hrthm.2004.07.001

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