Lahbib, Saida <br/><br/>
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology.  [electronic resource] 

 -  Journal of applied genetics  Feb 2019 
 - 49-56 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>2190-3883 
<br/><br/><label>Standard No.: </label>10.1007/s13353-018-0472-3  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Autism Spectrum Disorder--genetics<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 2--genetics<br/>Female<br/>GTPase-Activating Proteins--genetics<br/>Hearing Loss--genetics<br/>Homozygote<br/>Humans<br/>Infant<br/>Intellectual Disability--genetics<br/>Male<br/>Pedigree<br/>Sequence Deletion