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

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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.

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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

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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

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

21 January 2018

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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

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

21 January 2018

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

21 January 2018

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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

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

21 January 2018

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Sinus node dysfunction concomitant with Brugada syndrome

21 January 2018

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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

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21 January 2018

Identifiers

DOI

10.1111/JCE.12470

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23 July 2017

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