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Fragile X Syndrome, another NDD that is characterized by intellectual disability (ID) among other symptoms, has high comorbidity with ASD and is a result of a CGG triplet repeat expansion mutation in the fragile X mental retardation 1 gene ( FMR1 ) that silences the production of its encoded FMRP protein [45, 46]
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Keep it real: rethinking the primacy of experimental control in cognitive neuroscience
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