Delayed loss of UBE3A reduces the expression of Angelman syndrome-associated phenotypes

BACKGROUND: Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by mutations affecting UBE3A gene expression. Previous studies in mice revealed distinct critical periods during neurodevelopment in which reactivation of Ube3a gene expression can prevent the onset of behavioral defic...

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Detaylı Bibliyografya
Yayımlandı:Mol Autism
Asıl Yazarlar: Sonzogni, Monica, Hakonen, Johanna, Bernabé Kleijn, Mireia, Silva-Santos, Sara, Judson, Matthew C., Philpot, Benjamin D., van Woerden, Geeske M., Elgersma, Ype
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2019
Konular:
Short Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6532248/
https://ncbi.nlm.nih.gov/pubmed/31143434
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13229-019-0277-1
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