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Dysregulation of mTOR Signaling in Fragile X Syndrome

Fragile X syndrome, the most common form of inherited mental retardation and leading genetic cause of autism, is caused by transcriptional silencing of the Fmr1 gene. The fragile X mental retardation protein (FMRP), the gene product of Fmr1, is an RNA binding protein that negatively regulates transl...

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Detaylı Bibliyografya
Asıl Yazarlar: Sharma, Ali, Hoeffer, Charles A., Takayasu, Yukihiro, Miyawaki, Takahiro, McBride, Sean M., Klann, Eric, Zukin, R. Suzanne
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Society for Neuroscience 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3665010/
https://ncbi.nlm.nih.gov/pubmed/20071534
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3696-09.2010
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