(Q33154577)

English

A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death

scientific article published on 14 December 2006

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Europe PubMed Central

PubMed publication ID

22 July 2017

A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

long QT syndrome

1 reference

based on heuristic

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author name string

Yanmin Zhang

1

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Nan Zhou

2

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Wenhui Jiang

3

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Jun Peng

4

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Hongmei Wan

5

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Chen Huang

6

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

Zenghui Xie

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

Andrew A Grace

9

1 reference

Europe PubMed Central

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22 July 2017

Aiqun Ma

10

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

publication date

14 December 2006

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Europe PubMed Central

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22 July 2017

European Journal of Pediatrics

1 reference

Europe PubMed Central

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22 July 2017

166

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Europe PubMed Central

PubMed publication ID

22 July 2017

9

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Europe PubMed Central

PubMed publication ID

22 July 2017

927-933

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

The long QT syndrome. Prospective longitudinal study of 328 families

1 reference

https://api.crossref.org/works/10.1007%2FS00431-006-0346-2

21 January 2018

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.

1 reference

https://api.crossref.org/works/10.1007%2FS00431-006-0346-2

21 January 2018

Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

1 reference

https://api.crossref.org/works/10.1007%2FS00431-006-0346-2

21 January 2018

Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel KCNQ1 and HERG missense mutations in Dutch long-QT families

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac causes of sudden unexpected death in children and their relationship to seizures and syncope: genetic testing for cardiac electropathies

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation (T65P) in the PAS domain of the human potassium channel HERG results in the long QT syndrome by trafficking deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in HERG associated with notched T waves in long QT syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the hminK gene cause long QT syndrome and suppress IKs function

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile seizures and other epileptic phenotypes in a Chinese family with a missense mutation of KCNQ2

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A plethora of mechanisms in the HERG-related long QT syndrome. Genetics meets electrophysiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/17171344

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-006-0346-2

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 July 2017

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