Latest FMR1 Stories
Researchers have recently discovered that an expansion of DNA in patients with the common neurodegenerative disorder Fragile X-associated Tremor syndrome causes the production of an abnormal protein that is toxic to neurons.
An older, broad-spectrum antibiotic has shown “modest” yet meaningful improvements in general behavior, mood and anxiety for children suffering from fragile X syndrome.
While researchers have long been aware of a relationship between fragile X syndrome and autism, they have now begun to trace out the exact genetic pathways that link the two disorders together.
Neuroscientists at New York University have devised a method that has reduced several afflictions associated with Fragile X syndrome (FXS) in laboratory mice.
Researchers at Emory University School of Medicine have identified five rare mutations in a single gene that appear to increase the chances that a boy will develop an autism spectrum disorder (ASD).
The first U.S. population prevalence study of mutations in the gene that causes fragile X syndrome, the most common inherited form of intellectual disability, suggests the mutation in the gene – and its associated health risks – may be more common than previously believed.
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