Cargando…
Does function trump bioinformatics in Brugada syndrome-associated SCN5A mutation calling? Patients, computers, and patches
Autores principales: | Wilde, Arthur A M, Wu, Cheng-I |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8325777/ https://www.ncbi.nlm.nih.gov/pubmed/34333601 http://dx.doi.org/10.1093/eurheartj/ehab292 |
Ejemplares similares
-
SCN5A Mutations in Brugada Syndrome Are Associated with Increased Cardiac Dimensions and Reduced Contractility
por: van Hoorn, Frans, et al.
Publicado: (2012) -
SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families
por: Wijeyeratne, Yanushi D., et al.
Publicado: (2020) -
Compound Heterozygous SCN5A Mutations in Severe Sodium Channelopathy With Brugada Syndrome: A Case Report
por: Nijak, Aleksandra, et al.
Publicado: (2020) -
Novel SCN5A Frameshift Mutation in Brugada Syndrome Associated With Complex Arrhythmic Phenotype
por: Micaglio, Emanuele, et al.
Publicado: (2019) -
Sex‐Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome
por: Aizawa, Yoshiyasu, et al.
Publicado: (2018)