Genetic and maternal predictors of cognitive and behavioral trajectories in females with fragile X syndrome

BACKGROUND: Fragile X syndrome (FXS) is caused by a mutation in the FMR1 gene on the X chromosome, leading to decreased levels of FMR1 protein (FMRP), which causes the array of neuropsychological impairments that define FXS. Because FXS is an X-linked condition, fewer females display FXS and females...

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Detaylı Bibliyografya
Yayımlandı:J Neurodev Disord
Asıl Yazarlar: del Hoyo Soriano, Laura, Thurman, Angela John, Harvey, Danielle Jenine, Ted Brown, W., Abbeduto, Leonard
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2018
Konular:
Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6011256/
https://ncbi.nlm.nih.gov/pubmed/29925305
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-018-9240-2
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