Davis, L K <br/><br/>
Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jul 2012 
 - 1654-61 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.35396  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Autistic Disorder--complications<br/>Child<br/>DNA Copy Number Variations<br/>Gene Deletion<br/>Humans<br/>Male<br/>Paresis--complications<br/>Pedigree<br/>Phenotype<br/>RNA Splicing Factors<br/>RNA-Binding Proteins--genetics