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From circuits to behavior: Amygdala dysfunction in fragile X syndrome
Fragile X syndrome (FXS) is a neurodevelopmental disorder caused by a repeat expansion mutation in the promotor region of the FMR1 gene resulting in transcriptional silencing and loss of function of fragile X messenger ribonucleoprotein 1 protein (FMRP). FMRP has a well-defined role in the early dev...
Autores principales: | Svalina, Matthew N., Sullivan, Regina, Restrepo, Diego, Huntsman, Molly M. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034113/ https://www.ncbi.nlm.nih.gov/pubmed/36969493 http://dx.doi.org/10.3389/fnint.2023.1128529 |
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