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Temporal and regional differences in the olfactory proteome as a consequence of MeCP2 deficiency

Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the gene encoding MeCP2. By binding to methylated CpG dinucleotide promoter regions, MeCP2 acts as a transcriptional repressor, predicting that its absence might result in widespread aberrant gene transcription, leading to t...

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Autors principals: Matarazzo, Valéry, Ronnett, Gabriele V.
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2004
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC419680/
https://ncbi.nlm.nih.gov/pubmed/15128950
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0307083101
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