Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleDe novo heterozygous missense and loss‐of‐function variants in CDC42BPB are associated with a neurodevelopmental phenotype.AuthorsChilton, Ilana; Okur, Volkan; Vitiello, Giuseppina; Selicorni, Angelo; Mariani, Milena; Goldenberg, Alice; Husson, Thomas; Campion, Dominique; Lichtenbelt, Klaske D.; Gassen, Koen; Steinraths, Michelle; Rice, Jennifer; Roeder, Elizabeth R.; Littlejohn, Rebecca O.; Srour, Myriam; Sebire, Guillaume; Accogli, Andrea; Héron, Delphine; Heide, Solveig; Nava, CarolinePublicationAmerican Journal of Medical Genetics. Part A, 2020, Vol 182, Issue 5, p962ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.61505