Partially Dominant Mutant Channel Defect Corresponding with Intermediate LQT2 Phenotype
Author:
Publisher
Wiley
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1540-8159.2011.03222.x/fullpdf
Reference37 articles.
1. Pharmacogenetic considerations in diseases of cardiac ion channels;Anantharam;J Pharmacol Exp Ther,2003
2. Molecular aspects of the congenital and acquired Long QT Syndrome: Clinical implications;Saenen;J Mol Cell Cardiol,2008
3. The genetic basis of long QT and short QT syndromes: A mutation update;Hedley;Hum Mutat,2009
4. A family of potassium channel genes related to eag in Drosophila and mammals;Warmke;Proc Natl Acad Sci U S A,1994
5. A minK-HERG complex regulates the cardiac potassium current I(Kr);McDonald;Nature,1997
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