Heinzen, Erin L <br/><br/>
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.  [electronic resource] 

 -  American journal of human genetics  Aug 2012 
 - 293-302 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>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2012.06.016  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Epilepsy, Generalized--genetics<br/>Exome--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Genome-Wide Association Study<br/>Genotype<br/>Humans<br/>Molecular Sequence Data<br/>Sequence Alignment<br/>Sequence Analysis, DNA<br/>White People--genetics