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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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| Publicado no: | Front Mol Neurosci |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6380165/ https://ncbi.nlm.nih.gov/pubmed/30809123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2019.00033 |
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