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Long Qt Syndrome 2

Known as: LQT2 
National Institutes of Health

Related topics

Related topics

8 relations
Autosomal dominant inheritanceKCNH2, ALA614VALKCNH2, ARG582CYSSudden Cardiac Death

Broader (1)

Long QT Syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
LQT5 masquerading as LQT2: a dominant negative effect of KCNE1-D85N rare polymorphism on KCNH2 current.
AIMS KCNE1 encodes an auxiliary subunit of cardiac potassium channels. Loss-of-function variations in this gene have been… 
2009
2009
Adrenergic regulation of the rapid component of delayed rectifier K+ current: implications for arrhythmogenesis in LQT2 patients.
2009
2009
Pharmacological Enhancement of Cardiac Gap Junction Coupling Prevents Arrhythmias in Canine LQT2 Model
Gap junctions contribute to the transmural heterogeneity of repolarization in the normal heart and under conditions of prolonged… 
2007
2007
A missense mutation (G604S) in the S5/pore region of HERG causes long QT syndrome in a Chinese family with a high incidence of sudden unexpected death
Long QT syndrome (LQTS) is characterized by abnormalities in cardiac repolarization that lead to prolongation of the… 
2005
2005
Efficient genotyping for congenital long QT syndrome.
  • E. Kaufman
  • Journal of the American Medical Association (JAMA…
  • 2005
  • Corpus ID: 27447921
WITHIN THE PAST DECADE, INVESTIGATORS HAVE uncovered the genetic basis for multiple long QT syndromes (LQTSs). These include LQT1… 
2004
2004
Temporal repolarization lability differences among genotyped patients with the long QT syndrome.
2003
2003
Clinical features and management of congenital long QT syndrome: a report on 54 patients from a national registry
To assess the clinical features and the management of congenital long QT syndrome (LQTS) in China, we collected the clinical data… 
Review
2002
Review
2002
Differentiation between LQT1 and LQT2 patients and unaffected subjects using 24-hour electrocardiographic recordings.
2001
2001
Re-entrant cardiac arrhythmias in computational models of long QT myocardium.
The long QT syndrome (LQTS) is an inherited disorder in which repolarization of cardiac ventricular cells is prolonged. Patients… 
1999
1999
A mitochondrial DNA mutation cosegregates with the pathophysiological U wave.
In a family with long QT syndrome (LQT2), some individuals who did not harbor the HERG mutation had a prolonged QTU interval on… 
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