Compound Heterozygous Mutations in the SCN5A-Encoded Nav1.5 Cardiac Sodium Channel Resulting in Atrial Standstill and His-Purkinje System Disease
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference10 articles.
1. Mechanistic links between Na+ channel (SCN5A) mutations and impaired cardiac pacemaking in sick sinus syndrome;Butters;Circ Res,2010
2. Clinical and electrophysiological characteristics of atrial standstill;Nakazato;Pacing Clin Electrophysiol,1995
3. Homozygous mutation in SCN5A associated with atrial quiescence, recalcitrant arrhythmias, and poor capture thresholds;Lopez;Heart Rhythm,2011
4. A cardiac sodium channel mutation identified in Brugada syndrome associated with atrial standstill;Takehara;J Intern Med,2004
5. A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill;Groenewegen;Circ Res,2003
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1. Atrial Standstill in the Pediatric Population;JACC: Clinical Electrophysiology;2023-01
2. An Adolescent Patient with Sick Sinus Syndrome Complicated by Hypothyroidism Carrying an<i> SCN5A</i> Variant;International Heart Journal;2022-05-30
3. Phenotypes of mutations related to voltage‐dependent sodium channels on children and adolescents;Journal of Biochemical and Molecular Toxicology;2022-02-21
4. Clinical Spectrum of SCN5A Channelopathy in Children with Primary Electrical Disease and Structurally Normal Hearts;Genes;2021-12-22
5. Atrial standstill in the newborn: a case report;Russian Journal of Cardiology;2021-08-08
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