(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

1 reference

26 July 2017

23 September 2008

1 reference

26 July 2017

1 reference

26 July 2017

9

1 reference

26 July 2017

87

1 reference

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

26 July 2017

0 references

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