A homozygous SCN5A mutation associated with atrial standstill and sudden death

The cardiac sodium channel gene SCN5A and its gene product NaV1.5: Role in physiology and pathophysiology

(2015) Christiaan C. Veerman et al.   GENE

Compound Heterozygous Mutations in the SCN5A-Encoded Nav1.5 Cardiac Sodium Channel Resulting in Atrial Standstill and His-Purkinje System Disease

(2014) Shankar Baskar et al.   JOURNAL OF PEDIATRICS

Paralogue annotation identifies novel pathogenic variants in patients with Brugada syndrome and catecholaminergic polymorphic ventricular tachycardia

(2013) Roddy Walsh et al.   JOURNAL OF MEDICAL GENETICS

A novel SCN5A mutation V1340I in Brugada syndrome augmenting arrhythmias during febrile illness

(2009) Kaveh Samani et al.   HEART RHYTHM

Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A

(2009) Argelia Medeiros-Domingo et al.   HEART RHYTHM

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

(2009) Jamie D. Kapplinger et al.   HEART RHYTHM

Sodium channel mutations and arrhythmias

(2009) Yanfei Ruan et al.   Nature Reviews Cardiology

Implantable Cardioverter-Defibrillator Implantation in a Patient with Atrial Standstill

(2009) So Ra Park et al.   YONSEI MEDICAL JOURNAL