We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMolecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptomsAuthorsWilson, H LPublicationJournal of Medical Genetics, 2003, Vol 40, Issue 8, p575ISSN1468-6244Publication typearticleDOI10.1136/jmg.40.8.575