Novel mutations in domain I of SCN5A cause Brugada syndrome (Q44019185)

29 November 2017

title

Novel mutations in domain I of SCN5A cause Brugada syndrome (English)

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29 November 2017

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29 November 2017

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ORCID Public Data File 2021

29 November 2017

Josep Brugada

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Jeffrey A Towbin

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object named as

Jeffrey A Towbin

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29 November 2017

Pedro Brugada

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29 November 2017

Ramon Brugada

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29 November 2017

Robert Dumaine

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29 November 2017

Koonlawee Nademanee

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29 November 2017

Matteo Vatta

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29 November 2017

Neil E Bowles

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29 November 2017

Hua Li

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29 November 2017

publication date

1 April 2002

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Molecular Genetics and Metabolism

29 November 2017

published in

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29 November 2017

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29 November 2017

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29 November 2017

page(s)

317-324

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

29 November 2017

cites work

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Further characterization of the syndrome of right bundle branch block, ST segment elevation, and sudden cardiac death

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The Brugada syndrome: clinical, electrophysiologic and genetic aspects.

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Ion channels and ventricular arrhythmias: cellular and ionic mechanisms underlying the Brugada syndrome

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Arrhythmogenic Marker for the Sudden Unexplained Death Syndrome in Thai Men

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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

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Multiple mechanisms of Na+ channel--linked long-QT syndrome

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Molecular mechanism for an inherited cardiac arrhythmia

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Cardiac conduction defects associate with mutations in SCN5A

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A sodium-channel mutation causes isolated cardiac conduction disease

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A molecular link between the sudden infant death syndrome and the long-QT syndrome

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Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent

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Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome

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A single Na(+) channel mutation causing both long-QT and Brugada syndromes

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Electrophysiological characterization of SCN5A mutations causing long QT (E1784K) and Brugada (R1512W and R1432G) syndromes

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Enhanced Na(+) channel intermediate inactivation in Brugada syndrome

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"Brugada" syndrome: clinical data and suggested pathophysiological mechanism

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Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families

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Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts

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Detection of Numerous Y Chromosome Biallelic Polymorphisms by Denaturing High-Performance Liquid Chromatography

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Effects of III-IV linker mutations on human heart Na+ channel inactivation gating

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Structure and function of voltage‐gated sodium channels

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7 January 2021

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7 January 2021

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Identifiers

DOI

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29 November 2017

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