Sarcoplasmic Reticulum Ca
CPVT
Calcium
Inherited arrhythmias
LQTS
Ryanodine receptor
Sarcoplasmic reticulum
Journal
Biochemical pharmacology
ISSN: 1873-2968
Titre abrégé: Biochem Pharmacol
Pays: England
ID NLM: 0101032
Informations de publication
Date de publication:
06 2022
06 2022
Historique:
received:
18
03
2022
revised:
18
04
2022
accepted:
19
04
2022
pubmed:
2
5
2022
medline:
18
5
2022
entrez:
1
5
2022
Statut:
ppublish
Résumé
Inherited arrhythmias are the leading causes for cardiac arrest and sudden cardiac death (SCD). Other than ion channel mutations, inherited arrhythmias including catecholaminergic polymorphic ventricular tachycardia (CPVT), long QT syndrome (LQTS), idiopathic ventricular fibrillation (IVF) and arrhythmogenic right ventricular cardiomyopathy (ARVC/D) may also be instigated by genetic mutations of sarcoplasmic reticulum (SR) proteins, including ryanodine receptor type-2 (RyR2), calsequestrin 2, SR Ca
Identifiants
pubmed: 35490731
pii: S0006-2952(22)00153-8
doi: 10.1016/j.bcp.2022.115059
pii:
doi:
Substances chimiques
Ryanodine Receptor Calcium Release Channel
0
Calcium
SY7Q814VUP
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
115059Informations de copyright
Copyright © 2022 Elsevier Inc. All rights reserved.