The loss of Fragile X mental retardation protein (FMRP) causes Fragile X syndrome, the
most common inherited mental retardation and single gene cause of autism. Although …

Loss of Fragile X mental retardation protein (FMRP) leads to Fragile X syndrome (FXS), the
most common form of inherited intellectual disability and autism. Although the functions of …

The fragile X mental retardation protein (FMRP) plays an important role in normal brain
development. Absence of FMRP results in abnormal neuronal morphologies in a selected …

Fragile X mental retardation protein (FMRP) and its autosomal paralog FXR2P are selective
neuronal RNA-binding proteins, and mice that lack either protein exhibit cognitive deficits …

Fragile X mental retardation protein (FMRP) is the product of the fragile X mental retardation
1 gene (FMR1), a gene that—when epigenetically inactivated by a triplet nucleotide repeat …

Fragile X syndrome (FXS), resulting solely from the loss of function of the human fragile X
mental retardation 1 (hFMR1) gene, is the most common heritable cause of mental …

Fragile X syndrome (FXS) results in intellectual disability (ID) most often caused by silencing
of the fragile X mental retardation 1 (FMR1) gene. The resulting absence of fragile X mental …

Fragile X syndrome, as well as other forms of mental retardation and autism, is associated
with altered dendritic spine number and structure. Fragile X syndrome is caused by loss-of …

Fragile X syndrome (FXS) is the most common form of inherited mental retardation and is
caused by the loss of function for Fragile X Mental Retardation Protein (FMRP), a selective …

Fragile X syndrome (FXS) is the most common inherited form of mental retardation and a
leading genetic cause of autism. There is increasing evidence in both FXS and other forms …