Antzelevitch, C <br/><br/>
Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.  [electronic resource] 

 -  Journal of electrocardiology  2001 
 - 177-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0022-0736 
<br/><br/><label>Standard No.: </label>10.1054/jelc.2001.28865  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Cation Transport Proteins<br/>Child<br/>Child, Preschool<br/>DNA-Binding Proteins<br/>Death, Sudden, Cardiac--etiology<br/>ERG1 Potassium Channel<br/>Ether-A-Go-Go Potassium Channels<br/>Humans<br/>Infant<br/>KCNQ Potassium Channels<br/>KCNQ1 Potassium Channel<br/>Long QT Syndrome--genetics<br/>Mutation<br/>NAV1.5 Voltage-Gated Sodium Channel<br/>Potassium Channels--genetics<br/>Potassium Channels, Voltage-Gated<br/>Sodium Channels--genetics<br/>Sudden Infant Death--genetics<br/>Trans-Activators<br/>Transcriptional Regulator ERG<br/>Ventricular Fibrillation--genetics