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MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.
Hum Mol Genet. 2005 Apr 15;14(8):1049-58. doi: 10.1093/hmg/ddi097. Epub 2005 Mar 9.
Hum Mol Genet. 2005.
PMID: 15757975
Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons.
Smrt RD, Eaves-Egenes J, Barkho BZ, Santistevan NJ, Zhao C, Aimone JB, Gage FH, Zhao X.
Smrt RD, et al.
Neurobiol Dis. 2007 Jul;27(1):77-89. doi: 10.1016/j.nbd.2007.04.005. Epub 2007 Apr 27.
Neurobiol Dis. 2007.
PMID: 17532643
Free PMC article.
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