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.
Mark Bear and Sara Kornfeld-Sylla in Bear's lab at The Picower Institute for Learning and Memory at MIT. Numerous potential treatments for neurological conditions, including autism spectrum disorders, ...
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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