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Overlapping LQT1 and LQT2 Phenotype in a Patient with Long QT Syndrome Associated with Loss-of-Function Variations in KCNQ1 and KCNH2

โœ Scribed by Cordeiro, Jonathan M.; Perez, Guillermo J.; Pfeiffer, Ryan; Burashnikov, Elena; Borggrefe, Martin; Wolpert, Christian; Schimpf, Rainer; Antzelevitch, Charles


Book ID
119206776
Publisher
Biophysical Society
Year
2010
Tongue
English
Weight
40 KB
Volume
98
Category
Article
ISSN
0006-3495

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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