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Lateral habenula dysfunctions in Tm4sf2(−/y) mice model for neurodevelopmental disorder
Mutations in the TM4SF2 gene, which encodes TSPAN7, cause a severe form of intellectual disability (ID) often comorbid with autism spectrum disorder (ASD). Recently, we found that TM4SF2 loss in mice affects cognition. Here, we report that Tm4sf2(−/y) mice, beyond an ID-like phenotype, display alter...
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| Gepubliceerd in: | Neurobiol Dis |
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| Hoofdauteurs: | , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Academic Press
2021
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7840593/ https://ncbi.nlm.nih.gov/pubmed/33227491 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2020.105189 |
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