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TCF20 dysfunction leads to cortical neurogenesis defects and autistic‐like behaviors in mice
Recently, de novo mutations of transcription factor 20 (TCF20) were found in patients with autism by large‐scale exome sequencing. However, how TCF20 modulates brain development and whether its dysfunction causes ASD remain unclear. Here, we show that TCF20 deficits impair neurogenesis in mouse. TCF...
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| Gepubliceerd in: | EMBO Rep |
|---|---|
| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
John Wiley and Sons Inc.
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7403713/ https://ncbi.nlm.nih.gov/pubmed/32510763 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/embr.201949239 |
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