The SCN5A Gene Is a Predictor of Phenotype Severity in Brugada Syndrome: A Comprehensive Literature Review

OBJECTIVE: The purpose of this review was to ascertain whether patients with Brugada syndrome (BrS) having SCN5A mutations have a more severe clinical phenotype and prognosis than do patients without SCN5A mutations. METHODS: A comprehensive Scopus database search was conducted; studies were selecte...

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Detalles Bibliográficos
Autores principales: Deica, Andreea Valentina, Paduraru, Livia Florentina, Paduraru, Dan Nicolae, Andronic, Octavian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2022
Materias:
Systematic Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267483/
https://www.ncbi.nlm.nih.gov/pubmed/36446338
http://dx.doi.org/10.1159/000528375

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10267483/
https://www.ncbi.nlm.nih.gov/pubmed/36446338
http://dx.doi.org/10.1159/000528375

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