Does KCNE5 play a role in long QT syndrome?-Reference-Cited by-同舟云学术

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Does KCNE5 play a role in long QT syndrome?

Published:2004-07 Issue:1-2 Volume:345 Page:49-53
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Hofman-Bang Jacob,Jespersen Thomas,Grunnet Morten,Larsen Lars Allan,Andersen Paal Skytt,Kanters Jørgen Kim,Kjeldsen Keld,Christiansen Michael

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference15 articles.

1. The long QT syndrome: ion channel diseases of the heart;Ackerman;Mayo Clin. Proc.,1998

2. Molecular biology and the prolonged QT syndromes;Towbin;Am. J. Med.,2001

3. Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2;Splawski;Circulation,2000

4. Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death;Mohler;Nature,2003

5. Functional and clinical characterization of KCNJ2 mutations associated with LQT7 [Andersen syndrome];Tristani-Firouzi;J. Clin. Invest.,2002

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Mutations of Voltage-Gated Ionic Channels and Risk of Severe Cardiac Arrhythmias;ACTA CARDIOL SIN;2019

2. KCNE4 and KCNE5: K+ channel regulation and cardiac arrhythmogenesis;Gene;2016-11

3. KCNE5 Polymorphism rs697829 is Associated with QT Interval and Survival in Acute Coronary Syndromes Patients;Journal of Cardiovascular Electrophysiology;2011-10-10

4. The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study;Journal of Negative Results in BioMedicine;2011-10-03

5. KCNE5 ( KCNE1L ) Variants Are Novel Modulators of Brugada Syndrome and Idiopathic Ventricular Fibrillation;Circulation: Arrhythmia and Electrophysiology;2011-06

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