De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway

Asif M, Kaygusuz E, Shinawi M, Nickelsen A, Hsieh T-C, Wagle P, Budde B, Hochscherf J, Höhne W, Höning S, Lindenblatt D, Noegel A, Altmüller J, Thiele H, Motameny S, Segal I, Tinschert S, Samra N, Savatt J, Rudy N, Fortugno P, Krawitz P, Hurst A, Niefind K, Jose J, Brancati F, Nürnberg P, Hussain MS