Biliczki, Peter <br/><br/>
Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction.  [electronic resource] 

 -  Heart rhythm  Dec 2009 
 - 1792-801 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1556-3871 
<br/><br/><label>Standard No.: </label>10.1016/j.hrthm.2009.08.009  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Analysis of Variance<br/>Animals<br/>CHO Cells<br/>Canada<br/>Cell Line<br/>Cricetinae<br/>Cricetulus<br/>Death, Sudden, Cardiac--pathology<br/>Ether-A-Go-Go Potassium Channels--genetics<br/>Guinea Pigs<br/>Humans<br/>KCNQ1 Potassium Channel--genetics<br/>Long QT Syndrome--genetics<br/>Microscopy, Confocal<br/>Mutation, Missense<br/>Myocytes, Cardiac--physiology<br/>Phenotype<br/>Torsades de Pointes--genetics<br/>Transfection