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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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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2004
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| Acesso em linha: | 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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