Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour

Neurodevelopmental disorders are multi-faceted and can lead to intellectual disability, autism spectrum disorder and language impairment. Mutations in the Forkhead box FOXP1 gene have been linked to all these disorders, suggesting that it may play a central role in various cognitive and social proce...

Descripción completa

Detalles Bibliográficos
Autores principales: Bacon, C, Schneider, M, Le Magueresse, C, Froehlich, H, Sticht, C, Gluch, C, Monyer, H, Rappold, G A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419151/
https://www.ncbi.nlm.nih.gov/pubmed/25266127
http://dx.doi.org/10.1038/mp.2014.116

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4419151/
https://www.ncbi.nlm.nih.gov/pubmed/25266127
http://dx.doi.org/10.1038/mp.2014.116

Ejemplares similares