Congenital long QT syndrome caused by the F275S KCNQ1 mutation: Mechanism of impaired channel function-Reference-Cited by-同舟云学术

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Congenital long QT syndrome caused by the F275S KCNQ1 mutation: Mechanism of impaired channel function

Published:2009-02 Issue:1 Volume:380 Page:127-131
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Li Wei,Wang Qiu-fen,Du Rong,Xu Qiu-Mei,Ke Qin-Mei,Wang Bin,Chen Xue-Lin,Tian Li,Zhang Shou-Yan,Kang Cai-Lian,Guan Si-Ming,Yang Jun-Guo,Song Zi-Fang

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference35 articles.

1. Congenital long QT syndrome;Crotti;Orphanet J. Rare Dis.,2008

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

3. LQT4 gene: the “missing” ankyrin;Yong;Mol. Interv.,2003

4. Andersen’s syndrome mutation effects on the structure and assembly of the cytoplasmic domains of Kir2.1;Pegan;Biochemistry,2006

5. Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism;Splawski;Cell,2004

Cited by 7 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. Pharmacological Screening of Kv7.1 and Kv7.1/KCNE1 Activators as Potential Antiarrhythmic Drugs in the Zebrafish Heart;International Journal of Molecular Sciences;2023-07-28

2. Insights into Cardiac IKs (KCNQ1/KCNE1) Channels Regulation;International Journal of Molecular Sciences;2020-12-11

3. Predicting the Functional Impact of KCNQ1 Variants of Unknown Significance;Circulation: Cardiovascular Genetics;2017-10

4. Chronic Probucol Treatment Decreases the Slow Component of the Delayed-Rectifier Potassium Current in CHO Cells Transfected With KCNQ1 and KCNE1;Journal of Cardiovascular Pharmacology;2012-04

5. A Dual Mechanism for IKs Current Reduction by the Pathogenic Mutation KCNQ1-S277L;Pacing and Clinical Electrophysiology;2011-09-02

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