Genetic analysis of Brugada syndrome and congenital long-QT syndrome type 3 in the Chinese (Q34153714)

31 July 2017

title

Genetic analysis of Brugada syndrome and congenital long-QT syndrome type 3 in the Chinese (English)

1 reference

31 July 2017

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1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:20877689

22 July 2024

author name string

Peng Liang

1

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31 July 2017

Wenling Liu

2

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31 July 2017

Cuilan Li

3

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31 July 2017

Wuhua Tao

4

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31 July 2017

Lei Li

5

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31 July 2017

Dayi Hu

6

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31 July 2017

language of work or name

English

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20877689

22 July 2024

publication date

1 April 2010

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full work available at URL

31 July 2017

https://europepmc.org/articles/pmc2945207?pdf=render

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:20877689

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20877689/pdf/?tool=EBI

22 July 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:20877689

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20877689/?tool=EBI

22 July 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:20877689

https://europepmc.org/articles/PMC2945207

22 July 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:20877689

https://europepmc.org/articles/PMC2945207?pdf=render

22 July 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:20877689

Journal of Cardiovascular Disease Research

22 July 2024

published in

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31 July 2017

volume

1

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31 July 2017

issue

2

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31 July 2017

page(s)

69-74

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Reduced voltage dependence of inactivation in the SCN5A sodium channel mutation delF1617.

31 July 2017

cites work

1 reference

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Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

5 July 2018

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Non-equilibrium gating in cardiac Na channels: an original mechanism of arrhythmia

5 July 2018

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Brugada syndrome: a decade of progress

5 July 2018

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A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction.

5 July 2018

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Natural history of Brugada syndrome: insights for risk stratification and management

5 July 2018

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

5 July 2018

1 reference

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Evaluation and treatment of pediatric patients with congenital or acquired long QT interval syndromes

5 July 2018

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Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na( ) channel.

5 July 2018

1 reference

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Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

5 July 2018

1 reference

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

5 July 2018

1 reference

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Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.

5 July 2018

1 reference

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

5 July 2018

1 reference

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Novel LQT-3 mutation affects Na channel activity through interactions between alpha- and beta1-subunits

5 July 2018

1 reference

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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

5 July 2018

1 reference

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

5 July 2018

1 reference

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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

5 July 2018

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

5 July 2018

1 reference

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A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics

5 July 2018

1 reference

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Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

28 October 2018

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A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome

28 October 2018

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

28 October 2018

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Congenital long-QT syndrome caused by a novel mutation in a conserved acidic domain of the cardiac Na channel

28 October 2018

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Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes

28 October 2018

1 reference

12 December 2020

Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes

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12 December 2020

Secondary structure of the human cardiac Na channel C terminus: evidence for a role of helical structures in modulation of channel inactivation

1 reference

12 December 2020

Genomic organization of the human SCN5A gene encoding the cardiac sodium channel

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12 December 2020

Genetic analysis of Brugada syndrome in Israel: two novel mutations and possible genetic heterogeneity

1 reference

12 December 2020

Mutation analysis of potassium channel genes KCNQ1 and KCNH2 in patients with long QT syndrome

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12 December 2020

Identifiers

DOI

10.4103/0975-3583.64437

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31 July 2017

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31 July 2017

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