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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Bibliografiske detaljer
Main Authors: Lawson-Yuen, Amy, Liu, Daniel, Han, Liqun, Jiang, Zhichun I., Tsai, Guochuan E., Basu, Alo C., Picker, Jonathan, Feng, Jiamin, Coyle, Joseph T.
Format: Artigo
Sprog:Inglês
Udgivet: 2007
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Article
Online adgang: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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