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Fetal Atrioventricular Block and Postpartum Augmentative QT Prolongation in a Patient With Long-QT Syndrome With KCNQ1 Mutation

โœ Scribed by HIROSHI FURUSHIMA; MASAOMI CHINUSHI; AKINORI SATO; YOSHIFUSA AIZAWA; AKIRA KIKUCHI; KOICHI TAKAKUWA; KENICHI TANAKA


Book ID
109208457
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
334 KB
Volume
21
Category
Article
ISSN
1540-8167

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KCNQ1 and KCNH2 mutations associated wit
โœ Wenling Liu; Junguo Yang; Dayi Hu; Cailian Kang; Cuilan Li; Shuoyan Zhang; Ping ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 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