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The last 5 uploaded publications
Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathy
Tom Rossenbacker, Els Schollen, Cuno Kuipéri, Thomy de Ravel, Koenraad Devriendt, Gert Matthijs, Désiré Collen, Hein Heidbüchel, Peter Carmeliet (2005). Unconventional intronic splice site mutation in SCN5A associates with cardiac sodium channelopathy. , 42(5), DOI: https://doi.org/10.1136/jmg.2004.029058.
Article172 days agoNovel 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.
Article172 days agoUnconventional 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)
Article172 days ago