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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...

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Bibliografiske detaljer
Main Authors: Blue, Mary E., Kaufmann, Walter E., Bressler, Joseph, Eyring, Charlotte, O’Driscoll, Cliona, Naidu, SakkuBai, Johnston, Michael V.
Format: Artigo
Sprog:Inglês
Udgivet: 2011
Fag:
Online adgang: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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