Homozygous mutation in SCN5A associated with atrial quiescence, recalcitrant arrhythmias, and poor capture thresholds
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Reference13 articles.
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2. Atrial standstill: a paralysis of cardiological relevance;Marini;Ital Heart J Suppl,2004
3. Compound heterozygous SCN5A mutations: does the sum of the parts equal the whole?;Benson;Heart Rhythm,2009
4. Sodium channel gene (SCN5A) mutations in 44 index patients with Brugada syndrome: different incidences in familial and sporadic disease;Schulze-Bahr;Hum Mutat,2003
5. A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illness;Samani;Heart Rhythm,2009
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1. Atrial Standstill in the Pediatric Population;JACC: Clinical Electrophysiology;2023-01
2. Mutations in NaV1.5 Reveal Calcium-Calmodulin Regulation of Sodium Channel;Frontiers in Physiology;2019-06-05
3. Heritability in genetic heart disease: the role of genetic background;Open Heart;2019-05
4. Mechanisms in Heritable Sodium Channel Diseases;Cardiac Electrophysiology: From Cell to Bedside;2018
5. Switch From Fetal to Adult SCN5A Isoform in Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes Unmasks the Cellular Phenotype of a Conduction Disease–Causing Mutation;Journal of the American Heart Association;2017-07
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