Variants in the sodium voltage-gated channel alpha subunit 5 gene (SCN5A) produce variable cardiac phenotypes including Brugada syndrome, conduction disease and cardiomyopathy. These phenotypes can lead to life-threatening arrhythmias, heart failure, and sudden cardiac death. Novel variants in splice-site regions of SCN5A require functional studies to characterise their pathogenicity as they are poorly understood. The generation of an induced pluripotent stem cell line provides a valuable resource to investigate the functional effects of potential splice-disrupting variants in SCN5A
AbstractLoss-of-function mutations in the cardiac sodium channel α-subunit gene SCN5A result in mult...
Brugada syndrome predisposes to sudden death due to disruption of normal cardiac ion channel functio...
BACKGROUND: Primary dysrhythmias other than those associated with the long QT syndrome, are increasi...
BACKGROUND: Ventricular fibrillation is one of the leading causes of death in North America. Bru...
Brugada syndrome (BS) is an inherited cardiac disorder associated with a high risk of sudden cardiac...
The SCN5A gene encodes the alpha subunit of the human cardiac voltage-gated sodium channel. Mutation...
Background: Mutations in the cardiac sodium channel, SCN5A, have been associated with one type of lo...
The cardiac sodium channel (Nav1.5) controls cardiac excitability by triggering the action potential...
Introduction: Familial dilated cardiomyopathy (DCM) is clinically variable and has been associated w...
Aims Brugada syndrome (BrS) is characterized by arrhythmias leading to sudden cardiac death. BrS is ...
SCN5A gene encodes the pore-forming ion-conducting α-subunit of the cardiac sodium channel (Nav1.5),...
Introduction: Familial dilated cardiomyopathy (DCM) is clinically variable and has been associated w...
PubMed ID: 18464934Brugada syndrome is a genetic disease associated with sudden cardiac death that i...
Background: Brugada syndrome is an inherited arrhythmogenic disease characterized by right bundle br...
International audienceLoss-of-function mutations in the cardiac Na + channel α-subunit Na v 1.5, enc...
AbstractLoss-of-function mutations in the cardiac sodium channel α-subunit gene SCN5A result in mult...
Brugada syndrome predisposes to sudden death due to disruption of normal cardiac ion channel functio...
BACKGROUND: Primary dysrhythmias other than those associated with the long QT syndrome, are increasi...
BACKGROUND: Ventricular fibrillation is one of the leading causes of death in North America. Bru...
Brugada syndrome (BS) is an inherited cardiac disorder associated with a high risk of sudden cardiac...
The SCN5A gene encodes the alpha subunit of the human cardiac voltage-gated sodium channel. Mutation...
Background: Mutations in the cardiac sodium channel, SCN5A, have been associated with one type of lo...
The cardiac sodium channel (Nav1.5) controls cardiac excitability by triggering the action potential...
Introduction: Familial dilated cardiomyopathy (DCM) is clinically variable and has been associated w...
Aims Brugada syndrome (BrS) is characterized by arrhythmias leading to sudden cardiac death. BrS is ...
SCN5A gene encodes the pore-forming ion-conducting α-subunit of the cardiac sodium channel (Nav1.5),...
Introduction: Familial dilated cardiomyopathy (DCM) is clinically variable and has been associated w...
PubMed ID: 18464934Brugada syndrome is a genetic disease associated with sudden cardiac death that i...
Background: Brugada syndrome is an inherited arrhythmogenic disease characterized by right bundle br...
International audienceLoss-of-function mutations in the cardiac Na + channel α-subunit Na v 1.5, enc...
AbstractLoss-of-function mutations in the cardiac sodium channel α-subunit gene SCN5A result in mult...
Brugada syndrome predisposes to sudden death due to disruption of normal cardiac ion channel functio...
BACKGROUND: Primary dysrhythmias other than those associated with the long QT syndrome, are increasi...