Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome-Reference-Cited by-同舟云学术

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Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome

Published:2008-09 Issue:9 Volume:5 Page:1275-1281
ISSN:1547-5271
Container-title:Heart Rhythm
language:en
Short-container-title:Heart Rhythm

Author:

Eddy Carey-Anne,MacCormick Judith M.,Chung Seo-Kyung,Crawford Jackie R.,Love Donald R.,Rees Mark I.,Skinner Jonathan R.,Shelling Andrew N.

Publisher

Elsevier BV

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference29 articles.

1. Mechanisms of disease: ion channels. Basic science and clinical disease;Ackerman;N Engl J Med,1997

2. The long QT syndrome;Moss;Circulation,1991

3. Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1);Wilde;J Am Coll Cardiol,1999

4. Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias;Schwartz;Circulation,2001

5. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing;Tester;Heart Rhythm,2005

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1. From genes to clinical management: A comprehensive review of long QT syndrome pathogenesis and treatment;Heart Rhythm O2;2024-08

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3. Human Genetics of Cardiac Arrhythmias;Advances in Experimental Medicine and Biology;2024

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