Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?

Brugada syndrome is a rare inherited arrhythmogenic disease leading to ventricular fibrillation and high risk of sudden death. In 1998, this syndrome was linked with a genetic variant with an autosomal dominant pattern of inheritance. To date, rare variants identified in more than 40 genes have been...

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Detalles Bibliográficos
Autores principales: Campuzano, Oscar, Sarquella-Brugada, Georgia, Cesar, Sergi, Arbelo, Elena, Brugada, Josep, Brugada, Ramon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582739/
https://www.ncbi.nlm.nih.gov/pubmed/32998306
http://dx.doi.org/10.3390/ijms21197155

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582739/
https://www.ncbi.nlm.nih.gov/pubmed/32998306
http://dx.doi.org/10.3390/ijms21197155

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