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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...

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Detalles Bibliográficos
Autores principales: Svalina, Matthew N., Sullivan, Regina, Restrepo, Diego, Huntsman, Molly M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
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