Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleHeterozygous variants in SPTBN1 cause intellectual disability and autism.AuthorsRosenfeld, Jill A.; Xiao, Rui; Bekheirnia, Mir Reza; Kanani, Farah; Parker, Michael J.; Koenig, Mary K.; Haeringen, Arie; Ruivenkamp, Claudia; Rosmaninho‐Salgado, Joana; Almeida, Pedro M.; Sá, Joaquim; Pinto Basto, Jorge; Palen, Emily; Oetjens, Kathryn F.; Burrage, Lindsay C.; Xia, Fan; Liu, Pengfei; Eng, Christine M.; Yang, Yaping; Posey, Jennifer E.PublicationAmerican Journal of Medical Genetics. Part A, 2021, Vol 185, Issue 7, p2037ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.62201