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pdf MeCP2 def. in Rett synd. causes epigen. aberrations at PWS/AS impr. cent. th. affects UBE3A express. Populair

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

Kirill Makedonski et al

Human Molecular Genetics
2005, Vol. 14, No. 8
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