Pharmacology of the short QT syndrome N588K-hERG K+ channel mutation: differential impact on selected class I and class III antiarrhythmic drugs
Author:
Publisher
Wiley
Subject
Pharmacology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1038/bjp.2008.325/fullpdf
Reference44 articles.
1. Guide to Receptors and Channels (GRAC), 3rd edition;Alexander;Br J Pharmacol,2008
2. Mutation in the KCNQ1 gene leading to the short QT-interval syndrome;Bellocq;Circulation,2004
3. Sudden death associated with short-QT syndrome linked to mutations in HERG;Brugada;Circulation,2004
4. Position of aromatic residues in the S6 domain, not inactivation, dictates cisapride sensitivity of HERG and eag potassium channels;Chen;Proc Natl Acad Sci USA,2002
5. Modulation of IKr inactivation by mutation N588K in KCNH2: a link to arrhythmogenesis in short QT syndrome;Cordeiro;Cardiovasc Res,2005
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