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Social behavior in 16p11.2 and 22q11.2 copy number variations: Insights from mice and humans
Genetic 16p11.2 and 22q11.2 deletions and duplications in humans may alter behavioral developmental trajectories increasing the risk of autism and schizophrenia spectrum disorders, and of attention‐deficit/hyperactivity disorder. In this review, we will concentrate on 16p11.2 and 22q11.2 deletions&#...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Blackwell Publishing Ltd
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744525/ https://www.ncbi.nlm.nih.gov/pubmed/34889032 http://dx.doi.org/10.1111/gbb.12787 |