IRES
Research Article | SpotlighthnRNP Q Regulates Internal Ribosome Entry Site-Mediated fmr1 Translation in NeuronsFragile X syndrome (FXS) caused by loss of fragile X mental retardation protein (FMRP), is the most common cause of inherited intellectual disability. Numerous studies show that FMRP is an RNA binding protein that regulates translation of its binding targets and plays key roles in neuronal functions.