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Pediatric patient LQTS T2
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创建时间：
2023-01-03
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Additional file 1 of Myocardial bridging and de novo SCN5A variant: coincidence or cause in sudden cardiac death in the young?
Supplementary Material 1.
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Supplementary Material for: A Novel SCN5A Variant Associated with Abnormal Repolarization, Atrial Fibrillation, and Reversible Cardiomyopathy
A variety of life-threating arrhythmias are caused by mutations in the cardiac voltage-gated sodium channel encoded by the SCN5A gene. In this study, we report a novel loss-of-function SCN5A variant,
Figshare2018-04-10 更新20
Table 1_Genetic predisposition to immune dysregulation and extracellular matrix remodeling in cardiac arrhythmia reveals potential mediation by SPP1+ macrophages.xlsx
IntroductionCardiac arrhythmia frequently co-presents with structural abnormalities such as cardiomyopathy and myocardial fibrosis, creating a bidirectional relationship where electrical disturbances
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In vivo Ryr2 editing corrects catecholaminergic polymorphic ventricular tachycardia
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a lethal inherited arrhythmia disorder most commonly caused by missense mutations in the RyR2 gene. The goal of this study was to determ
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Distribution of KCNH2(1956,C>T)genotype and allele frequency in male and female patients.
Distribution of KCNH2(1956,C>T)genotype and allele frequency in male and female patients.
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