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Long Qt Syndrome 4

Known as: LQT4 
 
National Institutes of Health

Papers overview

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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… Expand
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2008
2008
Congenital LQTS comprises a distinct group of cardiac channelopathies characterized by delayed repolarization of the myocardium… Expand
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Highly Cited
2006
Highly Cited
2006
BACKGROUND Congenital long-QT syndrome (LQTS) is a primary arrhythmogenic syndrome stemming from perturbed cardiac repolarization… Expand
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Highly Cited
2006
Highly Cited
2006
BACKGROUND Mutations in the RyR2-encoded cardiac ryanodine receptor/calcium release channel and in CASQ2-encoded calsequestrin… Expand
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Highly Cited
2004
Highly Cited
2004
Long QT syndrome (LQTS) is a prototypic arrhythmic disorder that is characterised by prolonged QT interval (or QTc) on… Expand
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Review
2003
Review
2003
Mutations in ion channels have been implicated in the formation of long QT syndrome (LQTS). However, Mohler et al. have recently… Expand
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Highly Cited
1999
Highly Cited
1999
BACKGROUND The rate-corrected QT interval (QTc) is heritable, and the discovery of quantitative trait loci that influence the QTc… Expand
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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… Expand
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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… Expand
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1997
1997
Abstract The Romano Ward long QT syndrome (LQTS) has an autosomal dominant mode of inheritance. Patients suffer from syncopal… Expand
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