Hamdan, Fadi F <br/><br/>
De novo mutations in moderate or severe intellectual disability.  [electronic resource] 

 -  PLoS genetics  Oct 2014 
 - e1004772 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.1004772  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Codon, Nonsense<br/>Epilepsy--genetics<br/>Exome--genetics<br/>Frameshift Mutation<br/>Humans<br/>Intellectual Disability--genetics<br/>Mutation, Missense<br/>Point Mutation<br/>RNA Splicing--genetics<br/>Sequence Deletion