Grozeva, Detelina <br/><br/>
De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability.  [electronic resource] 

 -  American journal of human genetics  Apr 2014 
 - 618-24 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2014.03.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 3<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Methyltransferases--genetics<br/>Mutation