The Fragile X syndrome, caused by the absence or mutation of fragile X mental retardation protein, FMRP, is a the common component of inherited intellectual disability and autism. This SnapShot surveys the protein interaction partners of FMRP, focusing on the cellular pathways in which they are involved.
Pasciuto, E., & Bagni, C. (2014). SnapShot: FMRP Interacting Proteins. Cell, 159(1), 218-218.e1. https://doi.org/10.1016/j.cell.2014.08.036