Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNeurodevelopmental disorders: Fragile signalling.AuthorsYates, DarranAbstractThe article offers information on the study conducted related to fragile X syndrome, the most common genetic cause of autism, which arises from the loss of fragile X mental retardation protein (FMRP).SubjectsFRAGILE X syndrome; AUTISMPublicationNature Reviews Neuroscience, 2012, Vol 13, Issue 11, p739ISSN1471-003XPublication typeArticleDOI10.1038/nrn3375