Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleExpanding the phenotype of Seckel syndrome associated with biallelic loss‐of‐function variants in CEP63.AuthorsPekkola Pacheco, Nadja; Pettersson, Maria; Lindstrand, Anna; Grigelioniene, GiedrePublicationAmerican Journal of Medical Genetics. Part A, 2023, Vol 191, Issue 7, p1929ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.63200