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Trio Haploinsufficiency Causes Neurodevelopmental Disease–Associated Deficits
Heterozygous coding mutations in TRIO are associated with neurodevelopmental disorders, including autism, schizophrenia, bipolar disorder, and epilepsy, and impair TRIO’s biochemical activities. To model mutant alleles, we ablated one or both Trio alleles from excitatory neurons in the cortex and hi...
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| Publié dans: | Cell Rep |
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| Auteurs principaux: | , , , , , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6436967/ https://ncbi.nlm.nih.gov/pubmed/30840899 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2019.02.022 |
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