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...

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Detalles Bibliográficos
Autores principales: Herrero, Maria Jesus, Wang, Li, Hernandez-Pineda, David, Banerjee, Payal, Matos, Heidi Y., Goodrich, Meredith, Panigrahi, Aswini, Smith, Nathan Anthony, Corbin, Joshua G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Behavioral Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8374433/
https://www.ncbi.nlm.nih.gov/pubmed/34421555
http://dx.doi.org/10.3389/fnbeh.2021.706079

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8374433/
https://www.ncbi.nlm.nih.gov/pubmed/34421555
http://dx.doi.org/10.3389/fnbeh.2021.706079

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