(Q33148846)

22 July 2017

title

KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death (English)

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22 July 2017

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S Chen

1

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22 July 2017

L Zhang

2

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22 July 2017

R M Bryant

3

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22 July 2017

G M Vincent

4

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22 July 2017

M Flippin

5

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22 July 2017

J C Lee

6

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22 July 2017

E Brown

7

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22 July 2017

F Zimmerman

8

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22 July 2017

R Rozich

9

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22 July 2017

P Szafranski

10

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22 July 2017

C Oberti

11

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22 July 2017

R Sterba

12

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22 July 2017

D Marangi

13

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22 July 2017

P J Tchou

14

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22 July 2017

M K Chung

15

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22 July 2017

Q Wang

16

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22 July 2017

publication date

1 April 2003

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22 July 2017

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22 July 2017

volume

63

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22 July 2017

issue

4

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22 July 2017

page(s)

273-282

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A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN

22 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

21 June 2018

1 reference

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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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

Implantable cardioverter-defibrillator: beyond efficacy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

Another role for the sympathetic nervous system in 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=1579805

Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening 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=1579805

KCNE2 confers background current characteristics to the cardiac KCNQ1 potassium channel

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

Effectiveness and limitations of beta-blocker therapy in 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=1579805

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

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=1579805

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=1579805

Clinical implications for affected parents and siblings of probands with 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=1579805

Genomic organization and mutational analysis of KVLQT1, a gene responsible for familial long QT syndrome

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579805

CONGENITAL CARDIAC ARRHYTHMIA

31 October 2018

1 reference

12 December 2020

Role of transvenous implantable cardioverter-defibrillators in preventing sudden cardiac death in children, adolescents, and young adults

1 reference

12 December 2020

1 reference

12 December 2020

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

1 reference

12 December 2020

Low penetrance in the long-QT syndrome: clinical impact

1 reference

12 December 2020

10.1034/J.1399-0004.2003.00048.X

Identifiers

DOI

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22 July 2017

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22 July 2017

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