Helbig, Ingo <br/><br/>
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.  [electronic resource] 

 -  Nature genetics  Feb 2009 
 - 160-2 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>1546-1718 
<br/><br/><label>Standard No.: </label>10.1038/ng.292  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Case-Control Studies<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 15<br/>Comparative Genomic Hybridization<br/>Epilepsy, Generalized--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Humans<br/>Male<br/>Receptors, Nicotinic--genetics<br/>Risk Factors<br/>Young Adult<br/>alpha7 Nicotinic Acetylcholine Receptor