Lupoglazoff, Jean-Marc <br/><br/>
Long QT syndrome in neonates: conduction disorders associated with HERG mutations and sinus bradycardia with KCNQ1 mutations.  [electronic resource] 

 -  Journal of the American College of Cardiology  Mar 2004 
 - 826-30 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0735-1097 
<br/><br/><label>Standard No.: </label>10.1016/j.jacc.2003.09.049  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Bradycardia--genetics<br/>Cation Transport Proteins--genetics<br/>Ether-A-Go-Go Potassium Channels<br/>Female<br/>Follow-Up Studies<br/>Humans<br/>Infant, Newborn<br/>KCNQ Potassium Channels<br/>KCNQ1 Potassium Channel<br/>Long QT Syndrome--genetics<br/>Male<br/>Mutation<br/>Potassium Channels--genetics<br/>Potassium Channels, Voltage-Gated