Lal, Dennis <br/><br/>
Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies.  [electronic resource] 

 -  PLoS genetics  May 2015 
 - e1005226 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1553-7404 
<br/><br/><label>Standard No.: </label>10.1371/journal.pgen.1005226  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Case-Control Studies<br/>Child<br/>Cohort Studies<br/>DNA Copy Number Variations<br/>Epilepsy, Generalized--genetics<br/>Female<br/>Gene Rearrangement<br/>Genetic Association Studies<br/>Genome, Human<br/>Humans<br/>Male<br/>Neurodevelopmental Disorders--genetics<br/>Polymorphism, Single Nucleotide<br/>Protein Interaction Domains and Motifs<br/>Sequence Deletion<br/>Young Adult