Loss of Satb2 in the Cortex and Hippocampus Leads to Abnormal Behaviors in Mice

Satb2-associated syndrome (SAS) is a genetic disorder that results from the deletion or mutation of one allele within the Satb2 locus. Patients with SAS show behavioral abnormalities, including developmental delay/intellectual disability, hyperactivity, and symptoms of autism. To address the role of...

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Detalles Bibliográficos
Autores principales: Zhang, Qiong, Huang, Ying, Zhang, Lei, Ding, Yu-Qiang, Song, Ning-Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6380165/
https://www.ncbi.nlm.nih.gov/pubmed/30809123
http://dx.doi.org/10.3389/fnmol.2019.00033

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6380165/
https://www.ncbi.nlm.nih.gov/pubmed/30809123
http://dx.doi.org/10.3389/fnmol.2019.00033

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