British Heart Foundation (RG/15/15/31742)NIHR Biomedical Research Centre at Bart
BACKGROUND: Patients carrying the cardiac sodium channel (SCN5A) mutation 1795insD show sudden noctu...
Loss-of-function mutations in the cardiac Na+ channel α-subunit gene, SCN5A, cause Brugada syndrome ...
Abstract The Scn5a gene encodes the major pore‐forming Nav1.5 (α) subunit, of the voltage‐gated Na+ ...
A murine line with a haploinsufficiency in SCN5A has been used to model human Brugada syndrome: a di...
Brugada syndrome (BrS) is associated with ventricular tachycardia originating particularly in the ri...
AbstractObjectivesWe investigate the extent to which the electrocardiographic (ECG) properties of in...
Brugada syndrome is an inherited, rare cardiac arrhythmogenic disease, associated with sudden cardia...
International audienceAims: Loss-of-function of the cardiac sodium channel NaV1.5 is a common featur...
AIM: To test a hypothesis attributing arrhythmia in Brugada Syndrome to right ventricular (RV) outfl...
International audienceBoth gain- and loss-of-function mutations in the SCN5A gene, which encodes the...
Brugada Syndrome is a rare cardiac disease that leads to an increased risk of sudden cardiac death d...
Scn5a heterozygous null (Scn5a+/-) mice have historically been used to investigate arrhythmogenic me...
Funder: University of Surrey; Id: http://dx.doi.org/10.13039/501100003513Abstract: The Scn5a gene en...
International audienceLoss-of-function mutations in the cardiac Na + channel α-subunit Na v 1.5, enc...
Mutations of SCN5A gene, which encodes the α-subunit of the voltage-gated Na channel NaV1.5, underli...
BACKGROUND: Patients carrying the cardiac sodium channel (SCN5A) mutation 1795insD show sudden noctu...
Loss-of-function mutations in the cardiac Na+ channel α-subunit gene, SCN5A, cause Brugada syndrome ...
Abstract The Scn5a gene encodes the major pore‐forming Nav1.5 (α) subunit, of the voltage‐gated Na+ ...
A murine line with a haploinsufficiency in SCN5A has been used to model human Brugada syndrome: a di...
Brugada syndrome (BrS) is associated with ventricular tachycardia originating particularly in the ri...
AbstractObjectivesWe investigate the extent to which the electrocardiographic (ECG) properties of in...
Brugada syndrome is an inherited, rare cardiac arrhythmogenic disease, associated with sudden cardia...
International audienceAims: Loss-of-function of the cardiac sodium channel NaV1.5 is a common featur...
AIM: To test a hypothesis attributing arrhythmia in Brugada Syndrome to right ventricular (RV) outfl...
International audienceBoth gain- and loss-of-function mutations in the SCN5A gene, which encodes the...
Brugada Syndrome is a rare cardiac disease that leads to an increased risk of sudden cardiac death d...
Scn5a heterozygous null (Scn5a+/-) mice have historically been used to investigate arrhythmogenic me...
Funder: University of Surrey; Id: http://dx.doi.org/10.13039/501100003513Abstract: The Scn5a gene en...
International audienceLoss-of-function mutations in the cardiac Na + channel α-subunit Na v 1.5, enc...
Mutations of SCN5A gene, which encodes the α-subunit of the voltage-gated Na channel NaV1.5, underli...
BACKGROUND: Patients carrying the cardiac sodium channel (SCN5A) mutation 1795insD show sudden noctu...
Loss-of-function mutations in the cardiac Na+ channel α-subunit gene, SCN5A, cause Brugada syndrome ...
Abstract The Scn5a gene encodes the major pore‐forming Nav1.5 (α) subunit, of the voltage‐gated Na+ ...
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