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Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome

✍ Scribed by Grunnet, Morten; Behr, Elijah Raphael; Calloe, Kirstine; Hofman-Bang, Jacob; Till, Jan; Christiansen, Michael; McKenna, William John; Olesen, Søren-Peter; Schmitt, Nicole

Book ID
123154423
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
823 KB
Volume
2
Category
Article
ISSN
1547-5271

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✍ Wenling Liu; Junguo Yang; Dayi Hu; Cailian Kang; Cuilan Li; Shuoyan Zhang; Ping 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 285 KB

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