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STX209

Known as: STX-209 
National Institutes of Health

Papers overview

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2014
2014
Fragile X Syndrome (FXS) is a disorder caused by a congenital mutation of the FMR1 gene on the X chromosome. FXS is associated… 
2012
2012
study identified a complete loss of synaptic retinoic acid signaling and associated homeostatic plasticity in FXS mice 5 . It is…