(Q33159274)

English

Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Prevalence and spectrum of large deletions or duplications in the major long QT syndrome-susceptibility genes and implications for long QT syndrome genetic testing (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

long QT syndrome

1 reference

based on heuristic

inferred from title

Michael J Ackerman

6

object named as

Michael J Ackerman

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

4

object named as

Barbara Deal

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

author name string

David J Tester

1

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Amber J Benton

2

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Laura Train

3

1 reference

Europe PubMed Central

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23 July 2017

Linnea M Baudhuin

5

1 reference

Europe PubMed Central

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23 July 2017

language of work or name

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publication date

1 October 2010

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

American Journal of Cardiology

1 reference

Europe PubMed Central

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23 July 2017

106

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

1124-1128

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

Mutation of an A-kinase-anchoring protein causes long-QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

SCN4B-encoded sodium channel beta4 subunit in 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=2950837

21 June 2018

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

Prevalence of long-QT syndrome gene variants 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=2950837

21 June 2018

Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

Sudden infant death syndrome: how significant are the cardiac channelopathies?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

21 June 2018

Diagnostic criteria for the long QT syndrome. An update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

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=2950837

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=2950837

21 June 2018

Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

31 October 2018

Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2950837

31 October 2018

Exclusion of multiple candidate genes and large genomic rearrangements in SCN5A in a Dutch Brugada syndrome cohort

1 reference

https://pubmed.ncbi.nlm.nih.gov/20920651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Delineation of the phenotype associated with 7q36.1q36.2 deletion: long QT syndrome, renal hypoplasia and mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20920651

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AMJCARD.2010.06.022

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

ResearchGate publication ID

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