Cargando…
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome
BACKGROUND: The use of next-generation sequencing enables a rapid analysis of many genes associated with sudden cardiac death in diseases like Brugada Syndrome. Genetic variation is identified and associated with 30–35% of cases of Brugada Syndrome, with nearly 20–25% attributable to variants in SCN...
Autores principales: | Allegue, Catarina, Coll, Mònica, Mates, Jesus, Campuzano, Oscar, Iglesias, Anna, Sobrino, Beatriz, Brion, Maria, Amigo, Jorge, Carracedo, Angel, Brugada, Pedro, Brugada, Josep, Brugada, Ramon |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4521779/ https://www.ncbi.nlm.nih.gov/pubmed/26230511 http://dx.doi.org/10.1371/journal.pone.0133037 |
Ejemplares similares
-
Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology
por: Campuzano, Oscar, et al.
Publicado: (2014) -
Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?
por: Campuzano, Oscar, et al.
Publicado: (2020) -
Large Genomic Imbalances in Brugada Syndrome
por: Mademont-Soler, Irene, et al.
Publicado: (2016) -
Determining the Pathogenicity of Genetic Variants Associated with Cardiac Channelopathies
por: Campuzano, Oscar, et al.
Publicado: (2015) -
Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population
por: Martínez-Barrios, Estefanía, et al.
Publicado: (2022)