Visual motion processing deficits in infants with the fragile X premutation

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 cogniti...

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Detalles Bibliográficos
Autores principales: Gallego, Pamela K, Burris, Jessica L, Rivera, Susan M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121307/
https://www.ncbi.nlm.nih.gov/pubmed/25093044
http://dx.doi.org/10.1186/1866-1955-6-29

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121307/
https://www.ncbi.nlm.nih.gov/pubmed/25093044
http://dx.doi.org/10.1186/1866-1955-6-29

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