Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA new regulatory pathway for fragile X syndrome?AuthorsHansen, R. Scott; Laird, Charles D.AbstractDescribes a genetic regulatory pathway for fragile X syndrome. Clinical effects of hypertranscription; Epigenetic gene inactivation by DNA methylation and translation control; Increasing use of RNA interference as a tool for reverse genetics.SubjectsFRAGILE X syndrome; GENETIC regulationPublicationNature Medicine, 2002, Vol 8, Issue 11, p1204ISSN1078-8956Publication typeArticleDOI10.1038/nm1102-1204