(Q33165997)

23 July 2017

title

Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval (English)

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23 July 2017

0 references

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10

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23 July 2017

8

Tea Skaaby

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Jesper Hastrup Svendsen

14

Jesper Hastrup Svendsen

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Stig Haunsø

13

Stig Haunsø

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23 July 2017

Gustav Ahlberg

5

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Christian T Have

Christian Theil Have

2

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Morten Salling Olesen

Morten Salling Olesen

17

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Søren-Peter Olesen

Søren-Peter Olesen

9

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Torben Hansen

Torben Hansen

15

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Allan Linneberg

Allan Linneberg

11

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Oluf Borbye Pedersen

Oluf Pedersen

12

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Peter E Weeke

3

Peter Weeke

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23 July 2017

4

Jonas Bille Nielsen

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23 July 2017

6

Marie Balslev-Harder

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23 July 2017

1

Jonas Ghouse

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23 July 2017

7

Emil Vincent Appel

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23 July 2017

Jørgen Kim Kanters

16

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23 July 2017

publication date

9 July 2015

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23 July 2017

published in

European Heart Journal

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23 July 2017

volume

36

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23 July 2017

issue

37

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23 July 2017

page(s)

2523-2529

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HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.

23 July 2017

cites work

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The current role of next-generation DNA sequencing in routine care of patients with hereditary cardiovascular conditions: a viewpoint paper of the European Society of Cardiology working group on myocardial and pericardial diseases and members of the

21 January 2018

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New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

21 January 2018

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https://api.crossref.org/works/10.1093%2FEURHEARTJ%2FEHV297

High prevalence of genetic variants previously associated with LQT syndrome in new exome data

21 January 2018

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Prevalences of diabetes and impaired glucose regulation in a Danish population: the Inter99 study

21 January 2018

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A randomized non-pharmacological intervention study for prevention of ischaemic heart disease: baseline results Inter99.

21 January 2018

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Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes

21 January 2018

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Diagnostic criteria for the long QT syndrome. An update

21 January 2018

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Prevention of torsade de pointes in hospital settings: a scientific statement from the American Heart Association and the American College of Cardiology Foundation

21 January 2018

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Accuracy of the ICD-10 discharge diagnosis for syncope

21 January 2018

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PLINK: a tool set for whole-genome association and population-based linkage analyses

21 January 2018

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Prevalence of the congenital long-QT syndrome.

21 January 2018

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21 January 2018

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Long-QT syndrome after age 40.

21 January 2018

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Mutant caveolin-3 induces persistent late sodium current and is associated with long-QT syndrome

21 January 2018

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The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote

21 January 2018

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Diagnostic miscues in congenital long-QT syndrome

21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/EURHEARTJ/EHV297

1 reference

23 July 2017

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