We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression.AuthorsMakedonski K; Abuhatzira L; Kaufman Y; Razin A; Shemer RPublicationHuman molecular genetics, 2005, Vol 14, Issue 8, p1049ISSN0964-6906Publication typearticleDOI10.1093/hmg/ddi097