We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleRett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.AuthorsAmir RE; Van den Veyver IB; Wan M; Tran CQ; Francke U; Zoghbi HYPublicationNature genetics, 1999, Vol 23, Issue 2, p185ISSN1061-4036Publication typearticleDOI10.1038/13810