Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations (Q33371126)

26 July 2017

Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations (English)

1 reference

single-nucleotide polymorphism

26 July 2017

1 reference

Xianqin Zhang

1

1 reference

26 July 2017

Shenghan Chen

2

1 reference

26 July 2017

Li Zhang

3

1 reference

26 July 2017

Mugen Liu

4

1 reference

26 July 2017

Sharon Redfearn

5

1 reference

26 July 2017

Randall M Bryant

6

1 reference

26 July 2017

Carlos Oberti

7

1 reference

26 July 2017

G Michael Vincent

8

1 reference

26 July 2017

Qing K Wang

9

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26 July 2017

23 September 2008

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26 July 2017

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26 July 2017

9

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26 July 2017

87

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https://scigraph.springernature.com/pub.10.1186/1471-2350-9-87

26 July 2017

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cites work

Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570672

A novel mutation in human ether-a-go-go-related gene, alanine to proline at position 490, found in a large family with autosomal dominant long QT 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=2570672

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570672

KCNH2-K897T is a genetic modifier of latent congenital long-QT 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=2570672

KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias 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=2570672

Bradycardia-induced long QT syndrome caused by a de novo missense mutation in the S2-S3 inner loop of HERG.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570672

Functional effects of mutations in KvLQT1 that cause long QT 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=2570672

Four novel KVLQT1 and four novel HERG mutations in familial long-QT 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=2570672

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570672

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2570672

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT 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=2570672

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT 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=2570672

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT 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=2570672

An intronic mutation causes long QT syndrome.

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-87

Compound mutations: a common cause of severe long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-87

Association between HERG K897T polymorphism and QT interval in middle-aged Finnish women

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-87

Common Genetic Variation in KCNH2 Is Associated With QT Interval Duration

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-87

Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-87

A common polymorphism in KCNH2 (HERG) hastens cardiac repolarization

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-9-87

Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18808722

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18808722

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association of KCNQ1, KCNE1, KCNH2 and SCN5A polymorphisms with QTc interval length in a healthy population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18808722

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-9-87

1 reference

Dimensions Publication ID

26 July 2017

0 references

1 reference

26 July 2017

1 reference