Surber, Ralf <br/><br/>
Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel.  [electronic resource] 

 -  Cardiovascular research  Mar 2008 
 - 740-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0008-6363 
<br/><br/><label>Standard No.: </label>10.1093/cvr/cvm096  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Action Potentials<br/>Adolescent<br/>Adult<br/>Ajmaline--therapeutic use<br/>Animals<br/>Anti-Arrhythmia Agents--therapeutic use<br/>Bundle-Branch Block--drug therapy<br/>Cell Line<br/>Child<br/>DNA Mutational Analysis<br/>Death, Sudden, Cardiac--etiology<br/>Electrocardiography<br/>Female<br/>Gene Transfer Techniques<br/>Genetic Predisposition to Disease<br/>Humans<br/>Kinetics<br/>Lidocaine--therapeutic use<br/>Long QT Syndrome--drug therapy<br/>Lysine<br/>Male<br/>Muscle Proteins--drug effects<br/>Mutation<br/>Myocardium--metabolism<br/>NAV1.5 Voltage-Gated Sodium Channel<br/>Patch-Clamp Techniques<br/>Pedigree<br/>Sodium--metabolism<br/>Sodium Channels--drug effects<br/>Syncope--genetics<br/>Threonine<br/>Xenopus laevis