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DDI097
DDI097
http://dx.doi.org/10.1093/HMG/DDI097
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression
P356
Q28593334-DA5E4975-3F0C-421B-90D6-32AEC5BEDA60
P356
DDI097
http://dx.doi.org/10.1093/HMG/DDI097