Sex-Specific Social Behavior and Amygdala Proteomic Deficits in Foxp2+/− Mutant Mice

In humans, mutations in the transcription factor encoding gene, FOXP2, are associated with language and Autism Spectrum Disorders (ASD), the latter characterized by deficits in social interactions. However, little is known regarding the function of Foxp2 in male or female social behavior. Our previo...

Full description

Bibliographic Details
Main Authors: Maria Jesus Herrero, Li Wang, David Hernandez-Pineda, Payal Banerjee, Heidi Y. Matos, Meredith Goodrich, Aswini Panigrahi, Nathan Anthony Smith, Joshua G. Corbin
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-08-01
Series:Frontiers in Behavioral Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnbeh.2021.706079/full