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Article

Visual motion processing deficits in infants with the fragile X premutation

30 Jul 2014

Abstract excerpt

BACKGROUND: Fragile X syndrome (FXS) results from a trinucleotide repeat expansion (full mutation >200 cytosine-guanine-guanine (CGG) repeats) in the FMR1 gene, leading to a reduction or absence of the gene's protein product, fragile X mental retardation protein (FMRP), ultimately causing cognitive and behavioral impairments that are characteristic of the syndrome. In our previous work with infants and toddlers...

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PMID: 25093044
DOI: 10.1186/1866-1955-6-29

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