Publications - Rett Syndrome / Angelman Syndrome

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MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affect UBE3A expression Makedonski, K., Abuhatzira, L., Kaufman, Y., Razin, A. and Shemer, R. H. Mol. Genet. 14: 1049-1058, 2005. [paper]