(Q33164391)

23 July 2017

title

p.Y1449C SCN5A mutation associated with overlap disorder comprising conduction disease, Brugada syndrome, and atrial flutter (English)

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23 July 2017

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3

Jonathan Timperley

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23 July 2017

Sandeep S Hothi

1

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23 July 2017

Farhana Ara

series ordinal

2

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23 July 2017

publication date

23 July 2014

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Journal of Cardiovascular Electrophysiology

23 July 2017

published in

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23 July 2017

volume

26

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23 July 2017

issue

1

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23 July 2017

page(s)

93-97

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Proposed diagnostic criteria for the Brugada syndrome

23 July 2017

cites work

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Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Brugada syndrome 2012.

1 reference

Abrupt rate accelerations or premature beats cause life-threatening arrhythmias in mice with long-QT3 syndrome.

21 January 2018

1 reference

Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a

21 January 2018

1 reference

Cardiac sodium channel overlap syndromes: different faces of SCN5A mutations

21 January 2018

1 reference

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family

21 January 2018

1 reference

Phenotypic overlap of cardiac sodium channelopathies: individual-specific or mutation-specific?

21 January 2018

1 reference

A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia

21 January 2018

1 reference

The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel

21 January 2018

1 reference

Nav1.5/R1193Q polymorphism is associated with both long QT and Brugada syndromes

21 January 2018

1 reference

SCN5A R1193Q polymorphism associated with progressive cardiac conduction defects and long QT syndrome in a Chinese family

21 January 2018

1 reference

Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation

21 January 2018

1 reference

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

21 January 2018

1 reference

Na(+) channel mutation that causes both Brugada and long-QT syndrome phenotypes: a simulation study of mechanism

21 January 2018

1 reference

The primary arrhythmia syndromes: same mutation, different manifestations. Are we starting to understand why?

21 January 2018

1 reference

Prevalence of supraventricular tachyarrhythmias in a cohort of 115 patients with Brugada syndrome

21 January 2018

1 reference

Sinus node dysfunction concomitant with Brugada syndrome

21 January 2018

1 reference

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/JCE.12470

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23 July 2017

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