Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleFunctional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1-associated neurodevelopmental disorder (DAND) phenotype.AuthorsChen, Li; Jensik, Philip J.; Alaimo, Joseph T.; Walkiewicz, Magdalena; Berger, Seth; Roeder, Elizabeth; Faqeih, Eissa A.; Bernstein, Jonathan A.; Smith, Ann C. M.; Mullegama, Sureni V.; Saffen, David W.; Elsea, Sarah H.PublicationHuman Mutation, 2017, Vol 38, Issue 12, p1774ISSN1059-7794Publication typeArticleDOI10.1002/humu.23339