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Novel mutation in the KCNH2 gene associated with long QT syndrome

✍ Scribed by Silva, Doroteia; Miltenberger-Miltenyi, Gabriel; Correia, Maria José; Diogo, António Nunes


Book ID
122855589
Publisher
Elsevier
Year
2013
Tongue
Portuguese
Weight
829 KB
Volume
32
Category
Article
ISSN
0870-2551

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The long QT syndrome (LQTS) is a cardiac disorder characterized by prolongation of the QT interval on electrocardiograms (ECGs), syncope and sudden death caused by a specific ventricular tachyarrhythmia known as torsade de pointes. LQTS is caused by mutations in ion channel genes including the cardi