Llwytho...
Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett Syndrome
Rett Syndrome (RTT) is a devastating neurological disorder that is caused by mutations in the MECP2 gene. Mecp2-mutant mice have been used as a model system to study the disease mechanism. Our previous work has suggested that MeCP2 malfunction in neurons is the primary cause of RTT in the mouse. How...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
National Academy of Sciences
2005
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1194957/ https://ncbi.nlm.nih.gov/pubmed/16116096 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0506071102 |
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