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Severe changes in colon epithelium in the Mecp2-null mouse model of Rett syndrome
BACKGROUND: Rett syndrome is best known due to its severe and devastating symptoms in the central nervous system. It is produced by mutations affecting the Mecp2 gene that codes for a transcription factor. Nevertheless, evidence for MECP2 activity has been reported for tissues other than those of th...
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| Publicado no: | Mol Cell Pediatr |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5116442/ https://ncbi.nlm.nih.gov/pubmed/27868160 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40348-016-0065-3 |
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