Saenen, J B <br/><br/>
A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes.  [electronic resource] 

 -  Journal of molecular and cellular cardiology  Jul 2007 
 - 63-72 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-2828 
<br/><br/><label>Standard No.: </label>10.1016/j.yjmcc.2007.04.012  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Amino Acid Sequence<br/>Amino Acid Substitution--genetics<br/>Base Sequence<br/>Canada<br/>Cell Line<br/>Ether-A-Go-Go Potassium Channels--genetics<br/>Female<br/>Genetic Diseases, Inborn<br/>Humans<br/>Long QT Syndrome--genetics<br/>Netherlands<br/>Pedigree<br/>Phenotype<br/>Point Mutation<br/>White People