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Pharmacological Modulation of AMPAR Rescues Intellectual Disability-Like Phenotype in Tm4sf2(−/y) Mice
Intellectual disability affects 2–3% of the world's population and typically begins during childhood, causing impairments in social skills and cognitive abilities. Mutations in the TM4SF2 gene, which encodes the TSPAN7 protein, cause a severe form of intellectual disability, and currently, no t...
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| Yayımlandı: | Cereb Cortex |
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| Asıl Yazarlar: | , , , , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5939231/ https://ncbi.nlm.nih.gov/pubmed/28968657 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhx221 |
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