Association of Mouse <i>Dlg4</i> (PSD-95) Gene Deletion and Human <i>DLG4</i> Gene Variation With Phenotypes Relevant to Autism Spectrum Disorders and Williams' Syndrome

Abstract

These findings demonstrate that DLG4 gene disruption in mice produces a complex range of behavioral and molecular abnormalities relevant to autism spectrum disorders and Williams' syndrome. The study provides an initial link between human DLG4 gene variation and key neural endophenotypes of Williams' syndrome and perhaps corticoamygdala regulation of emotional and social processes more generally.