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Altered cortical Cytoarchitecture in the Fmr1 knockout mouse
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by silencing of the FMR1 gene and subsequent loss of its protein product, fragile X retardation protein (FMRP). One of the most robust neuropathological findings in post-mortem human FXS and Fmr1 KO mice is the abnormal increase in den...
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| Publicado no: | Mol Brain |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6570929/ https://ncbi.nlm.nih.gov/pubmed/31200759 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-019-0478-8 |
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