A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation
出版年份 2013 全文链接
标题
A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation
作者
关键词
-
出版物
CARDIOVASCULAR RESEARCH
Volume 98, Issue 3, Pages 488-495
出版商
Oxford University Press (OUP)
发表日期
2013-02-12
DOI
10.1093/cvr/cvt028
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation
- (2012) Morten S Olesen et al. BMC Medical Genetics
- Genetic Loci on Chromosomes 4q25, 7p31, and 12p12 Are Associated With Onset of Lone Atrial Fibrillation Before the Age of 40 Years
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- High Prevalence of Long QT Syndrome–Associated SCN5A Variants in Patients With Early-Onset Lone Atrial Fibrillation
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- Novel mutations in the KCND3-encoded Kv4.3 K+ channel associated with autopsy-negative sudden unexplained death
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- Chromosome 4q25 Variants Are Genetic Modifiers of Rare Ion Channel Mutations Associated With Familial Atrial Fibrillation
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- SCN1Bb R214Q found in 3 patients: 1 with Brugada syndrome and 2 with lone atrial fibrillation
- (2011) Morten S. Olesen et al. HEART RHYTHM
- Comparison of the Effects of a Transient Outward Potassium Channel Activator on Currents Recorded from Atrial and Ventricular Cardiomyocytes
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- Effect of the Ito activator NS5806 on cloned Kv4 channels depends on the accessory protein KChIP2
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- Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation
- (2010) Morten S. Olesen et al. CARDIOVASCULAR RESEARCH
- Monogenic atrial fibrillation as pathophysiological paradigms
- (2010) S. Mahida et al. CARDIOVASCULAR RESEARCH
- Closed-state inactivation in Kv4.3 isoforms is differentially modulated by protein kinase C
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- Genetics of familial atrial fibrillation
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- Lone atrial fibrillation: what do we know?
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- Molecular determinants of cardiac transient outward potassium current (Ito) expression and regulation
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- A transient outward potassium current activator recapitulates the electrocardiographic manifestations of Brugada syndrome
- (2008) K. Calloe et al. CARDIOVASCULAR RESEARCH
- KCNE3 Mutation V17M Identified in a Patient with Lone Atrial Fibrillation
- (2008) Alicia Lundby et al. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
- Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome
- (2008) Eva Delpón et al. Circulation-Arrhythmia and Electrophysiology
- Cellular bases for human atrial fibrillation
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