Brugada syndrome genetics is associated with phenotype severity

AIMS : Brugada syndrome (BrS) is associated with an increased risk of sudden cardiac death due to ventricular tachycardia/fibrillation (VT/VF) in young, otherwise healthy individuals. Despite SCN5A being the most commonly known mutated gene to date, the genotype–phenotype relationship is poorly unde...

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Vydáno v:Eur Heart J
Hlavní autoři: Ciconte, Giuseppe, Monasky, Michelle M, Santinelli, Vincenzo, Micaglio, Emanuele, Vicedomini, Gabriele, Anastasia, Luigi, Negro, Gabriele, Borrelli, Valeria, Giannelli, Luigi, Santini, Francesca, de Innocentiis, Carlo, Rondine, Roberto, Locati, Emanuela T, Bernardini, Andrea, Mazza, Beniamino C, Mecarocci, Valerio, Ćalović, Žarko, Ghiroldi, Andrea, D’Imperio, Sara, Benedetti, Sara, Di Resta, Chiara, Rivolta, Ilaria, Casari, Giorgio, Petretto, Enrico, Pappone, Carlo
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2020
Témata:
Clnical Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7955973/
https://ncbi.nlm.nih.gov/pubmed/33221895
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/eurheartj/ehaa942
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