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Mecp2 truncation in male mice promotes affiliative social behavior
Mouse models of Rett syndrome, with targeted mutations in the Mecp2 gene, show a high degree of phenotypic consistency with the clinical syndrome. In addition to severe and age-specific regression in motor and cognitive abilities, a variety of studies have demonstrated that Mecp2 mutant mice display...
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| Vydáno v: | Behav Genet |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5843946/ https://ncbi.nlm.nih.gov/pubmed/21909962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10519-011-9501-2 |
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