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Ube3a mRNA and protein expression are not decreased in Mecp2(R168X) mutant mice
Mutations in the transcriptional repressor methyl CpG binding protein 2 (MeCP2) are responsible for most cases of Rett Syndrome (RS), a severe neurodevelopmental disorder characterized by developmental regression, minimal speech, seizures, postnatal microcephaly and hand sterotypies. Absence of the...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2706140/ https://ncbi.nlm.nih.gov/pubmed/17936729 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2007.08.039 |
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