Mohler, Peter J <br/><br/>
Defining the cellular phenotype of "ankyrin-B syndrome" variants: human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes.  [electronic resource] 

 -  Circulation  Jan 2007 
 - 432-41 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1524-4539 
<br/><br/><label>Standard No.: </label>10.1161/CIRCULATIONAHA.106.656512  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Animals<br/>Ankyrins--genetics<br/>Arrhythmias, Cardiac--chemically induced<br/>Asian People--genetics<br/>Black People--genetics<br/>Cytoskeleton--physiology<br/>Female<br/>Genetic Variation<br/>Genotype<br/>Humans<br/>Ion Channels--physiology<br/>Long QT Syndrome--chemically induced<br/>Male<br/>Mexican Americans--genetics<br/>Mice<br/>Mice, Inbred C57BL<br/>Middle Aged<br/>Myocytes, Cardiac--cytology<br/>Phenotype<br/>Tachycardia, Ventricular--chemically induced<br/>Torsades de Pointes--chemically induced<br/>White People--genetics