Brugada Syndrome: More than a Monogenic Channelopathy

Brugada syndrome (BrS) is an inherited cardiac channelopathy first diagnosed in 1992 but still considered a challenging disease in terms of diagnosis, arrhythmia risk prediction, pathophysiology and management. Despite about 20% of individuals carrying pathogenic variants in the SCN5A gene, the iden...

Descripción completa

Detalles Bibliográficos
Autores principales: Liantonio, Antonella, Bertini, Matteo, Mele, Antonietta, Balla, Cristina, Dinoi, Giorgia, Selvatici, Rita, Mele, Marco, De Luca, Annamaria, Gualandi, Francesca, Imbrici, Paola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452102/
https://www.ncbi.nlm.nih.gov/pubmed/37626795
http://dx.doi.org/10.3390/biomedicines11082297

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10452102/
https://www.ncbi.nlm.nih.gov/pubmed/37626795
http://dx.doi.org/10.3390/biomedicines11082297

Ejemplares similares