Torrico, Bārbara <br/><br/>
Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability.  [electronic resource] 

 -  European journal of human genetics : EJHG  Dec 2015 
 - 1694-701 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2015.37  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Autism Spectrum Disorder--genetics<br/>Case-Control Studies<br/>Cell Line, Tumor<br/>Female<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation, Missense<br/>Polymorphism, Single Nucleotide<br/>Promoter Regions, Genetic<br/>Trinucleotide Repeats