Polysomnographic Findings in Fragile X Syndrome Children with EEG Abnormalities

Fragile X syndrome (FXS) is a genetic syndrome with intellectual disability due to the loss of expression of the FMR1 gene located on chromosome X (Xq27.3). This mutation can suppress the fragile X mental retardation protein (FMRP) with an impact on synaptic functioning and neuronal plasticity. Amon...

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Detaylı Bibliyografya
Yayımlandı:Behav Neurol
Asıl Yazarlar: Carotenuto, Marco, Roccella, Michele, Pisani, Francesco, Matricardi, Sara, Verrotti, Alberto, Farello, Giovanni, Operto, Francesca Felicia, Bitetti, Ilaria, Precenzano, Francesco, Messina, Giovanni, Ruberto, Maria, Ciunfrini, Cristiana, Riccardi, Mariagrazia, Merolla, Eugenio, Pastorino, Grazia Maria Giovanna, Polito, Anna Nunzia, Marotta, Rosa
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Hindawi 2019
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6915005/
https://ncbi.nlm.nih.gov/pubmed/31885726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/5202808
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