Associated Papers
Genetic Testing in Brugada Syndrome: A 30-Year Experience.
Pannone L et al.
Circulation. Arrhythmia and Electrophysiology, 2024
38426305 (PubMed )
Supplement: circae_circae-2023-012374_supp1.pdf
Genetic testing in children with Brugada syndrome: results from a large prospective registry.
Pannone L et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology, 2023
A novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada syndrome.
Tarradas A et al.
Plos One, 2013
23308164 (PubMed )
Supplement: pone.0053220.s002.doc
Novel sodium channel SCN5A mutations in Brugada syndrome patients from Greece.
Kotta CM et al.
International Journal of Cardiology, 2010
Effects of mutations and genetic overlap in inherited long-QT and Brugada arrhythmia syndromes.
Kotta CM et al.
Hellenic Journal of Cardiology : Hjc = Hellenike Kardiologike Epitheorese, 0
Select a paper to view details