Tom Rossenbacker

Unconventional splice site mutation in SCN5A as cause (and modifier?) of overlapping phenotypes of Brugada syndrome and isolated cardiac conduction defect

Tom Rossenbacker, Els Schollen, Cuno Kuipéri, Thomy de Ravel, Gert Matthijs, Hein Heidbüchel, Peter Carmeliet (2004). Unconventional splice site mutation in SCN5A as cause (and modifier?) of overlapping phenotypes of Brugada syndrome and isolated cardiac conduction defect. , 110(17)