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Long QT syndrome in neonates: Conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations

✍ Scribed by Jean-Marc Lupoglazoff; Isabelle Denjoy; Elisabeth Villain; Véronique Fressart; Françoise Simon; André Bozio; Myriam Berthet; Nawal Benammar; Bernard Hainque; Pascale Guicheney


Book ID
119263770
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
263 KB
Volume
43
Category
Article
ISSN
1558-3597

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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