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

by Abdullah, U., Altmüller, J., Asif, M., Brancati, F., Budde, B.S, De Luca, C., Fleischer, N., Hochscherf, J., Höning, S., Hsieh, T.-C, Hurst, A.C.E, Hussain, M.S, Italian Undiagnosed Diseases Network, Jose, J., Kaygusuz, E., Krawitz, P., Lindenblatt, D., Motameny, S., Nickelsen, A., Niefind, K., Nienberg, C., Noegel, A.A, Nürnberg, P., Pais, L., Paola Fortugno, Rudy, N.L, Samra, N.N, Savatt, J.M, Segal, I., Shinawi, M., Thiele, H., Tinschert, S., Wagle, P., White, S.M
Published 2022