(Q33147371)

22 July 2017

Variable expression of long QT syndrome among gene carriers from families with five different HERG mutations (English)

1 reference

22 July 2017

1 reference

4

Wojciech Zareba

1 reference

22 July 2017

7

Jeffrey A Towbin

1 reference

22 July 2017

Jesaia Benhorin

1

1 reference

22 July 2017

Arthur J Moss

2

1 reference

22 July 2017

Matthew Bak

3

1 reference

22 July 2017

Elizabeth S Kaufman

5

1 reference

22 July 2017

Batsheva Kerem

6

1 reference

22 July 2017

Silvia Priori

8

1 reference

22 July 2017

Robert S Kass

9

1 reference

22 July 2017

Bernard Attali

10

1 reference

22 July 2017

Arthur M Brown

11

1 reference

22 July 2017

Eckhard Ficker

12

1 reference

22 July 2017

1 January 2002

1 reference

Annals of Noninvasive Electrocardiology

22 July 2017

1 reference

22 July 2017

7

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22 July 2017

1

1 reference

22 July 2017

40-46

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22 July 2017

The long Q-T syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

The long QT syndrome. Prospective longitudinal study of 328 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

The long-QT syndrome Genetic considerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

Nonparametric Estimation from Incomplete Observations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

HERG channel dysfunction in human long QT syndrome. Intracellular transport and functional defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

Electrocardiographic Prediction of Abnormal Genotype in Congenital Long QT Syndrome: Experience in 101 Related Family Members

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1542-474X.2001.TB00137.X

Novel characteristics of a misprocessed mutant HERG channel linked to hereditary long QT syndrome.

21 January 2018

1 reference

12 December 2020

Long QT syndrome: more questions

1 reference

12 December 2020

ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

1 reference

12 December 2020

A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN

1 reference

12 December 2020

Low penetrance in the long-QT syndrome: clinical impact

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with long QT syndrome

1 reference

12 December 2020

10.1111/J.1542-474X.2001.TB00137.X

Identifiers

DOI

1 reference

22 July 2017

1 reference