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Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome

โœ Scribed by C. Eddy; J. M. Maccormick; S. Chung; J. R. Crawford; D. R. Love; M. I. Rees; J. R. Skinner; A. N. Shelling


Book ID
121786660
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
967 KB
Volume
5
Category
Article
ISSN
1547-5271

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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