(Q33153667)

22 July 2017

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

1 reference

22 July 2017

0 references

H Huang

1

1 reference

22 July 2017

Juan Zhao

2

1 reference

22 July 2017

Fatima-Zahra Barrane

3

1 reference

22 July 2017

Jean Champagne

4

1 reference

22 July 2017

Mohamed Chahine

5

1 reference

22 July 2017

1 March 2006

1 reference

The Canadian Journal of Cardiology

22 July 2017

1 reference

22 July 2017

22

1 reference

22 July 2017

309-313

1 reference

22 July 2017

4

1 reference

Near-miss SIDS due to Brugada syndrome

22 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

Proposed diagnostic criteria for the Brugada syndrome: consensus report

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

The molecular genetics of the long QT syndrome: genes causing fainting and sudden death

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

Right bundle-branch block and ST-segment elevation in leads V1 through V3: a marker for sudden death in patients without demonstrable structural heart disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

Mapping of a gene for long QT syndrome to chromosome 4q25-27

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

R1193Q of SCN5A, a Brugada and long QT mutation, is a common polymorphism in Han Chinese

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

Molecular basis of the long-QT syndrome associated with deafness.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2560523

Restriction sites containing CpG show a higher frequency of polymorphism in human DNA

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16568155

12 December 2020

inferred from PubMed ID database lookup

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16568155

12 December 2020

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/16568155

12 December 2020

inferred from PubMed ID database lookup

Author's reply: link of SCN5A SNP R1193Q to long QT syndrome.

1 reference

Crossref

https://api.crossref.org/works/10.1016%2FS0828-282X%2806%2970915-1

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1016/S0828-282X(06)70915-1

1 reference

22 July 2017

1 reference

22 July 2017

1 reference