Changes in social behavior with MAPK2 and KCTD13/CUL3 pathways alterations in two new outbred rat models for the 16p11.2 syndromes with autism spectrum disorders

Copy number variations (CNVs) of the human 16p11.2 locus are associated with several developmental/neurocognitive syndromes. Particularly, deletion and duplication of this genetic interval are found in patients with autism spectrum disorders, intellectual disability and other psychiatric traits. The...

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Detalles Bibliográficos
Autores principales: Martin Lorenzo, Sandra, Muniz Moreno, Maria del Mar, Atas, Helin, Pellen, Marion, Nalesso, Valérie, Raffelsberger, Wolfgang, Prevost, Geraldine, Lindner, Loic, Birling, Marie-Christine, Menoret, Séverine, Tesson, Laurent, Negroni, Luc, Concordet, Jean-Paul, Anegon, Ignacio, Herault, Yann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350633/
https://www.ncbi.nlm.nih.gov/pubmed/37465586
http://dx.doi.org/10.3389/fnins.2023.1148683

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350633/
https://www.ncbi.nlm.nih.gov/pubmed/37465586
http://dx.doi.org/10.3389/fnins.2023.1148683

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