Long Qt Syndrome 4

Known as: LQT4 
 

Topic mentions per year

Topic mentions per year

1997-2013
01219972013

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2013
2013
1.3 Name of the analysed genes or DNA/chromosome segments LQT1: KCNQ1, 11p15.5; LQT2: KCNH2, 7q35-q36; LQT3: SCN5A, 3p21; LQT4… (More)
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2008
2008
s g t q a a I r m t g L m s L Congenital long QT syndrome (LQTS) comprises a disinct group of cardiac channelopathies that are… (More)
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Review
2008
Review
2008
Long-QT syndrome (LQTS) is an inherited disorder with prolonged ventricular repolarization and an increased propensity to… (More)
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2006
2006
BACKGROUND Mutations in the RyR2-encoded cardiac ryanodine receptor/calcium release channel and in CASQ2-encoded calsequestrin… (More)
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2004
2004
During recent years, genetic manipulations in the mouse aimed to settle animal models of cardiac channelopathies. Among this… (More)
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Review
2000
Review
2000
INTRODUCTION Progress in molecular genetics contributed to the discovery of pathophysiologic mechanisms of hereditary diseases as… (More)
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1999
1999
BACKGROUND The rate-corrected QT interval (QTc) is heritable, and the discovery of quantitative trait loci that influence the QTc… (More)
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1998
1998
BACKGROUND Long-QT syndrome (LQTS) is an inherited cardiac arrhythmia that causes sudden death in young, otherwise healthy people… (More)
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1998
1998
The long QT syndrome (LQT) is an inherited cardiac disorder that can cause sudden cardiac death among apparently healthy young… (More)
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1997
1997
The Romano Ward long QT syndrome (LQTS) has an autosomal dominant mode of inheritance. Patients suffer from syncopal attacks… (More)
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