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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Detalles Bibliográficos
Autores principales: Lee, Frankie H. F., Lai, Terence K. Y., Su, Ping, Liu, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6570929/
https://www.ncbi.nlm.nih.gov/pubmed/31200759
http://dx.doi.org/10.1186/s13041-019-0478-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6570929/
https://www.ncbi.nlm.nih.gov/pubmed/31200759
http://dx.doi.org/10.1186/s13041-019-0478-8

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