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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Detalles Bibliográficos
Autores principales: Ricci, Maria Teresa, Menegon, Silvia, Vatrano, Simona, Mandrile, Giorgia, Cerrato, Natascia, Carvalho, Paula, De Marchi, Mario, Gaita, Fiorenzo, Giustetto, Carla, Giachino, Daniela Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377327/
https://www.ncbi.nlm.nih.gov/pubmed/25253298
http://dx.doi.org/10.1038/srep06470

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5377327/
https://www.ncbi.nlm.nih.gov/pubmed/25253298
http://dx.doi.org/10.1038/srep06470

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