Heterozygous de novo variants in <scp> <i>CSNK1G1</i> </scp> are associated with syndromic developmental delay and autism spectrum disorder
Nina B. Gold(Harvard University), Elizabeth Bhoj(Children's Hospital of Philadelphia), Ilaria Parenti(University of Duisburg-Essen), Feliciano J. Ramos(Universidad de Zaragoza), Reem Saadeh‐Haddad(Georgetown University), Juan Pié(Universidad de Zaragoza), Frank J. Kaiser(Essen University Hospital), Lance H. Rodan(Boston Children's Hospital), María J. Guillen Sacoto, Anna Chassevent(Kennedy Krieger Institute), Hong Cui(University of Toronto), Kirsty McWalter, Dong Li(Children's Hospital of Philadelphia), Tim M. Strom(Ludwig-Maximilians-Universität München), Beatriz Puisac(Universidad de Zaragoza), Edward Blair(Nuffield Orthopaedic Centre), Constance Smith‐Hicks(Kennedy Krieger Institute)
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