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

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scientific article published in April 2002

Language	Label	Description	Also known as
English	Novel mutations in domain I of SCN5A cause Brugada syndrome	scientific article published in April 2002

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

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

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Europe PubMed Central

PubMed publication ID

29 November 2017

Charles Antzelevitch

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Europe PubMed Central

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29 November 2017

Charles Antzelevitch

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29 November 2017

object named as

Josep Brugada

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ORCID Public Data File 2021

Jeffrey A Towbin

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object named as

Jeffrey A Towbin

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29 November 2017

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object named as

Pedro Brugada

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29 November 2017

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object named as

Ramon Brugada

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29 November 2017

2

object named as

Robert Dumaine

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Europe PubMed Central

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29 November 2017

Koonlawee Nademanee

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object named as

Koonlawee Nademanee

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Europe PubMed Central

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29 November 2017

1

object named as

Matteo Vatta

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29 November 2017

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object named as

Neil E Bowles

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29 November 2017

author name string

Hua Li

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29 November 2017

publication date

1 April 2002

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29 November 2017

Molecular Genetics and Metabolism

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29 November 2017

75

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29 November 2017

4

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29 November 2017

317-324

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29 November 2017

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

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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

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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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https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

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inferred from DOI database lookup

The Brugada syndrome: clinical, electrophysiologic and genetic aspects.

1 reference

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7 January 2021

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

1 reference

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

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Arrhythmogenic Marker for the Sudden Unexplained Death Syndrome in Thai Men

1 reference

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

1 reference

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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

1 reference

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A sodium-channel mutation causes isolated cardiac conduction disease

1 reference

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

1 reference

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7 January 2021

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inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Enhanced Na(+) channel intermediate inactivation in Brugada syndrome

1 reference

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based on heuristic

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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

1 reference

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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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A routine method for the establishment of permanent growing lymphoblastoid cell lines

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Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

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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

1 reference

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7 January 2021

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Structure and function of voltage‐gated sodium channels

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Brugada syndrome and sudden cardiac death in children

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900006-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular biology of arrhythmic syndromes

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac arrhythmias: the genetic connection

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S1096-7192(02)00006-9

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 November 2017

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