O'Roak, B J <br/><br/>
Recurrent de novo mutations implicate novel genes underlying simplex autism risk.  [electronic resource] 

 -  Nature communications  Nov 2014 
 - 5595 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2041-1723 
<br/><br/><label>Standard No.: </label>10.1038/ncomms6595  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Autistic Disorder--genetics<br/>Base Sequence<br/>Carrier Proteins--genetics<br/>DNA-Binding Proteins--genetics<br/>Family<br/>Genetic Predisposition to Disease<br/>Humans<br/>Intelligence--genetics<br/>Intelligence Tests<br/>Mutation<br/>PAX5 Transcription Factor--genetics<br/>Risk<br/>Sequence Analysis, DNA<br/>Ubiquitin-Protein Ligases--genetics<br/>ras GTPase-Activating Proteins--genetics