To understand differences in neural activity between FXS and non-FXS individuals when responding to different frequencies, Thorpe said, researchers played an auditory “chirp,” or sound stimulus, and ...
Mutations in FMR1, the gene encoding fragile X messenger ribonucleoprotein 1 (FMRP), located at Xq27.3 and discovered in 1991, are the leading single-gene causes of autism and intellectual disability.
The cover artistically integrates multiple elements central to investigating the developmental origins of Fragile X syndrome. A vibrant DNA double helix structure rendered in rainbow iridescent colors ...
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