(Q33156531)

English

The cardiac sodium channel mutation delQKP 1507-1509 is associated with the expanding phenotypic spectrum of LQT3, conduction disorder, dilated cardiomyopathy, and high incidence of youth sudden death

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

The cardiac sodium channel mutation delQKP 1507-1509 is associated with the expanding phenotypic spectrum of LQT3, conduction disorder, dilated cardiomyopathy, and high incidence of youth sudden death (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

dilated cardiomyopathy

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

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author name string

Ruiming Shi

1

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Yanmin Zhang

2

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Chun Yang

3

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Chen Huang

4

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Xihui Zhou

5

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Hua Qiang

6

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Andrew A Grace

7

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Christopher L-H Huang

8

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Aiqun Ma

9

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

publication date

12 August 2008

1 reference

Europe PubMed Central

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22 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

1329-1335

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Overlap syndrome of cardiac sodium channel disease in mice carrying the equivalent mutation of human SCN5A-1795insD

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Sodium channel variants in heart disease: expanding horizons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Contribution of sodium channel mutations to bradycardia and sinus node dysfunction in LQT3 families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Genetic control of sodium channel function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Possible bradycardic mode of death and successful pacemaker treatment in a large family with features of long QT syndrome type 3 and Brugada syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Arrhythmogenic mechanism of an LQT-3 mutation of the human heart Na(+) channel alpha-subunit: A computational analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Familial automaticity-conduction disorder with associated cardiomyopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Amino acid residues required for fast Na(+)-channel inactivation: charge neutralizations and deletions in the III-IV linker

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

21 June 2018

Mutation detection in long QT syndrome: a comprehensive set of primers and PCR conditions

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUN202

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUN202

21 January 2018

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUN202

21 January 2018

Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death

1 reference

https://api.crossref.org/works/10.1093%2FEUROPACE%2FEUN202

21 January 2018

Cardiac sodium channel dysfunction in sudden infant death syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

31 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2573028

31 October 2018

Identifiers

10.1093/EUROPACE/EUN202

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

ResearchGate publication ID

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