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The neural circuit basis of Rett syndrome
Rett syndrome is an Autism Spectrum Disorder caused by mutations in the gene encoding methyl-CpG binding protein (MeCP2). Following a period of normal development, patients lose learned communication and motor skills, and develop a number of symptoms including motor disturbances, cognitive impairmen...
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| Asıl Yazarlar: | , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4079093/ https://ncbi.nlm.nih.gov/pubmed/24999353 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11515-012-1248-5 |
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