Class I antiarrhythmic drugs inhibit human cardiac two-pore-domain K+ (K2P) channels

Author:

Schmidt Constanze,Wiedmann Felix,Schweizer Patrick A.,Becker Rüdiger,Katus Hugo A.,Thomas Dierk

Funder

University of Heidelberg, Faculty of Medicine (Rahel Goitein-Straus Scholarship to CS)

German Cardiac Society (Otto Hess Scholarship to FW)

German Heart Foundation/German Foundation of Heart Research

Joachim Siebeneicher Foundation (to DT)

DZHK (Deutsches Zentrum für Herz-Kreislauf-Forschung – German Centre for Cardiovascular Research)

BMBF (German Ministry of Education and Research) (to HAK and DT)

Max-Planck-Society (TANDEM project to PAS)

Publisher

Elsevier BV

Subject

Pharmacology

Reference60 articles.

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4. Effect of CYP2D6⁎10 genotype on propafenone pharmacodynamics in Chinese patients with ventricular arrhythmia;Cai;Acta Pharmacologica Sinica,2002

5. 2012 focused update of the ESC Guidelines for the management of atrial fibrillation: an update of the 2010 ESC Guidelines for the management of atrial fibrillation. Developed with the special contribution of the European Heart Rhythm Association;Camm;European Heart Journal,2012

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