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Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice
Our previous postmortem study of girls with Rett Syndrome (RTT), a development disorder caused by MECP2 mutations, found increases in the density of NMDA receptors in the prefrontal cortex of 2–8 year-old girls, while girls older than 10 years had reductions in NMDA receptors compared to age matched...
Gorde:
| Egile Nagusiak: | , , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2011
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4122218/ https://ncbi.nlm.nih.gov/pubmed/21901842 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ar.21380 |
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