학술논문
De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway
Document Type
Article
Author
Asif, M.; Budde, B.S.; Altmüller, J.; Thiele, H.; Motameny, S.; Nürnberg, P.; Hussain, M.S.; Kaygusuz, E.; Höning, S.; Noegel, A.A.; Shinawi, M.; Nickelsen, A.; Nienberg, C.; Jose, J.; Hsieh, T.-C.; Krawitz, P.; Wagle, P.; Hochscherf, J.; Lindenblatt, D.; Niefind, K.; Abdullah, U.; Fleischer, N.; Segal, I.; Samra, N.N.; Pais, L.; Tinschert, S.; Savatt, J.M.; Rudy, N.L.; Hurst, A.C.E.; De Luca, C.; Paola Fortugno; Brancati, F.; White, S.M.
Source
In: Human Genetics and Genomics Advances . (Human Genetics and Genomics Advances, 14 July 2022, 3(3))
Subject
Language
English
ISSN
26662477