Congenital Long QT syndrome and torsade de pointes
Author:
Affiliation:
1. Downstate Medical Center; State University of New York; Brooklyn NY USA
2. VA NY Harbor Healthcare System; Brooklyn NY USA
3. NewYork-Presbyterian Brooklyn Methodist Hospital; New York NY USA
4. NYU School of Medicine; New York NY USA
Funder
Narrows Institute for Biomedical Research and Education
Biomedical Laboratory Research and Development, VA Office of Research and Development
Publisher
Wiley
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/anec.12481/fullpdf
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3. Molecular genetics of arrhythmias and cardiovascular conditions associated with arrhythmias;Antzelevitch;Journal of Cardiovascular Electrophysiology,2003
4. A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization;Arking;Nature Genetics,2006
5. K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current;Barhanin;Nature,1996
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