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Criteria to predict carriers of a novel SCN5A mutation in a large Portuguese family affected by the Brugada syndrome

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2012 Europace.pdf206.24 KBAdobe PDF Download

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Abstract(s)

Brugada syndrome (BrS) is a life-threatening arrhythmia disorder associated with autosomal-dominant mutations in the SCN5A gene. We aimed to characterize the diagnostic challenges and clinical manifestations of a novel SCN5A mutation associated with BrS.

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Brugada Syndrome SCN5A mutation ECG SAECG Diagnostic criteria Sudden cardiac death

Citation

Santos, L. F., Rodrigues, B., Moreira, D., Correia, E., Nunes, L., Costa, A., Elvas, L., Pereira, T., Machado, J. C., Henriques, C., Matos, A. & Santos, J. O. (2012). Criteria to predict carriers of a novel SCN5A mutation in a large Portuguese family affected by the Brugada syndrome. Europace, 14(6), 882–8

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