Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleDe novo, heterozygous, loss-of-function mutations in SYNGAP1 cause a syndromic form of intellectual disability.AuthorsParker, Michael J.; Fryer, Alan E.; Shears, Deborah J.; Lachlan, Katherine L.; McKee, Shane A.; Magee, Alex C.; Mohammed, Shehla; Vasudevan, Pradeep C.; Park, Soo‐Mi; Benoit, Valérie; Lederer, Damien; Maystadt, Isabelle; study, DDD; FitzPatrick, David R.PublicationAmerican Journal of Medical Genetics. Part A, 2015, Vol 167A, Issue 10, p2231ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.37189