Fragile X syndrome (FXS) is a developmental disorder caused by a mutation in the X‐linked
FMR1 gene, coding for the FMRP protein which is largely involved in synaptic function. FXS …

Fragile X syndrome (FXS) is a major developmental disorder and the most frequent
monogenic cause of autism. Surprisingly, most existing studies on the Fmr1‐KO mouse …

Fragile X syndrome (FXS) is the most common single gene cause of autism and intellectual
disabilities. Humans with FXS exhibit increased anxiety, sensory hypersensitivity, seizures …

Summary Fragile X Syndrome (FXS) is a commonly inherited form of intellectual disability
and one of the leading genetic causes for autism spectrum disorder. Clinical symptoms of …

Fragile X syndrome (FXS) is the most common inherited form of intellectual disability in
humans. In addition to cognitive impairment, patients may exhibit hyperactivity, attention …

Autism is a pervasive developmental disorder appearing before the age of 3, where
communication and social interactions are impaired. It also entails stereotypic behavior or …

Fragile X Syndrome is the most common form of inherited mental retardation. It is also
known for having a substantial behavioral morbidity, including autistic features. In humans …

Fragile X syndrome (FXS) is a monogenic disease caused by mutations in the FMR1 gene.
The Fmr1 knockout (KO) mice show many aspects of FXS-related phenotypes, and have …

The Fragile X syndrome (FXS) is the most frequent form of inherited mental disability and is
considered a monogenic cause of autism spectrum disorder. FXS is caused by a triplet …

Since the fragile X mental retardation 1 (FMR1) gene was sequenced in 1991 (1), there
have been a flurry of papers which have investigated molecular clinical correlations in both …