Lehnart, Stephan E <br/><br/>
Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function.  [electronic resource] 

 -  Circulation  Nov 2007 
 - 2325-45 p.  digital 
<br/><br/> Publication Type: Consensus Development Conference, NIH; Journal Article 
<br/><br/><label>ISSN: </label>1524-4539 
<br/><br/><label>Standard No.: </label>10.1161/CIRCULATIONAHA.107.711689  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Arrhythmias, Cardiac--diagnosis<br/>Cardiomyopathies--diagnosis<br/>Channelopathies--diagnosis<br/>Humans<br/>Long QT Syndrome--diagnosis<br/>Mutation<br/>National Heart, Lung, and Blood Institute (U.S.)<br/>Phenotype<br/>United States