Tau reduction attenuates autism-like features in Fmr1 knockout mice
Abstract Background Fragile X syndrome (FXS) is a leading cause of autism spectrum disorder (ASD) and resulted from a loss of the FMR1-encoded fragile X messenger ribonucleoprotein 1 (FMRP) protein due to large CGG repeat expansions in the promoter region of the FMR1 gene. The microtubule-associated...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMC
2023-11-01
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| Col·lecció: | Molecular Autism |
| Matèries: | |
| Accés en línia: | https://doi.org/10.1186/s13229-023-00574-1 |
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