Unravelling Novel
Brugada syndrome
Nav1.5
SCN5A
arrhythmias
automated patch clamp
mexiletine
sodium channel
sudden cardiac death
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
11 Oct 2023
11 Oct 2023
Historique:
received:
08
09
2023
revised:
08
10
2023
accepted:
09
10
2023
medline:
30
10
2023
pubmed:
28
10
2023
entrez:
28
10
2023
Statut:
epublish
Résumé
Brugada Syndrome (BrS) is a rare inherited cardiac arrhythmia causing potentially fatal ventricular tachycardia or fibrillation, mainly occurring during rest or sleep in young individuals without heart structural issues. It increases the risk of sudden cardiac death, and its characteristic feature is an abnormal ST segment elevation on the ECG. While BrS has diverse genetic origins, a subset of cases can be conducted to mutations in the
Identifiants
pubmed: 37894777
pii: ijms242015089
doi: 10.3390/ijms242015089
pmc: PMC10606416
pii:
doi:
Substances chimiques
SCN5A protein, human
0
NAV1.5 Voltage-Gated Sodium Channel
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Ricerca Corrente funding from the Italian Ministry of Health to IRCCS Policlinico San Donato, and by the University of Milano-Bicocca, 2016-CONT-0494
ID : 2016-CONT-0494
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