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Alessandra M Linardi

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Correa-Velloso J, Linardi A, Glaser T, Velloso F, Rivas M, Leite R, et al.
BMC Neurosci . 2022 Jun; 23(1):32. PMID: 35641906
Background: Fragile X syndrome, the major cause of inherited intellectual disability among men, is due to deficiency of the synaptic functional regulator FMR1 protein (FMRP), encoded by the FMRP translational...