(Q58011012)

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Gene-specific lethality of arrhythmic events in the long QT syndrome? A message from the International Registry

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title

Gene-specific lethality of arrhythmic events in the long QT syndrome? A message from the International Registry (English)

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publication date

1 August 1999

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published in

European Heart Journal

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volume

20

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issue

16

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page(s)

1137-1139

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cites work

The long Q-T syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

Idiopathic long QT syndrome: progress and questions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

Molecular mechanism for an inherited cardiac arrhythmia

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

Multiple mechanisms of Na+ channel--linked long-QT syndrome.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

Lidocaine block of LQT-3 mutant human Na+ channels

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

The long QT syndrome. Prospective longitudinal study of 328 families

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

The idiopathic long QT syndrome: the need for a prospective registry

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1053%2FEUHJ.1999.1511

retrieved

21 January 2018

Identifiers

DOI

10.1053/EUHJ.1999.1511

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PubMed ID

10448016

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(Q58011012)

Gene-specific lethality of arrhythmic events in the long QT syndrome? A message from the International Registry

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