Guo, Youling <br/><br/>
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.  [electronic resource] 

 -  Human molecular genetics  Mar 2012 
 - 1184-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddr550  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Asian People--genetics<br/>Child<br/>Child, Preschool<br/>Cytoskeletal Proteins--genetics<br/>Epilepsy--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Genome-Wide Association Study<br/>Humans<br/>Male<br/>Microtubule-Associated Proteins<br/>Middle Aged<br/>Odds Ratio<br/>Polymorphism, Single Nucleotide<br/>Young Adult