In vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylation

Fragile X syndrome (FXS), caused by loss of the Fragile X Mental Retardation 1 (FMR1) gene product (FMRP), is the most common heritable cause of intellectual disability and autism spectrum disorders. It has been long hypothesized that the phosphorylation of serine 500 (S500) in human FMRP controls i...

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Bibliographic Details
Main Authors: Coffee, R. Lane, Williamson, Ashley J., Adkins, Christopher M., Gray, Marisa C., Page, Terry L., Broadie, Kendal
Format: Artigo
Language:Inglês
Published: Oxford University Press 2012
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Articles
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3263990/
https://ncbi.nlm.nih.gov/pubmed/22080836
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr527
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