MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.

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@article{Makedonski2005MeCP2DI, title={MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.}, author={Kirill Makedonski and Liron Abuhatzira and Yotam Kaufman and Aharon Razin and Ruth Shemer}, journal={Human molecular genetics}, year={2005}, volume={14 8}, pages={1049-58} }