Boczek, Nicole J <br/><br/>
Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndrome.  [electronic resource] 

 -  Circulation. Cardiovascular genetics  Jun 2013 
 - 279-89 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>1942-3268 
<br/><br/><label>Standard No.: </label>10.1161/CIRCGENETICS.113.000138  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Base Sequence<br/>Calcium Channels, L-Type--genetics<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Exome<br/>Female<br/>Genes, Dominant<br/>Humans<br/>Long QT Syndrome--genetics<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Pedigree<br/>Young Adult