SCN1B gene variants in Brugada Syndrome: a study of 145 SCN5A-negative patients

Brugada syndrome is characterised by a typical ECG with ST segment elevation in the right precordial leads. Individuals with this condition are susceptible to ventricular arrhythmias and sudden cardiac death. The principal gene responsible for this syndrome is SCN5A, which encodes the α-subunit of t...

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Bibliographic Details
Published in:Sci Rep
Main Authors: Ricci, Maria Teresa, Menegon, Silvia, Vatrano, Simona, Mandrile, Giorgia, Cerrato, Natascia, Carvalho, Paula, De Marchi, Mario, Gaita, Fiorenzo, Giustetto, Carla, Giachino, Daniela Francesca
Format: Artigo
Language:Inglês
Published: Nature Publishing Group 2014
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Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5377327/
https://ncbi.nlm.nih.gov/pubmed/25253298
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep06470
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