• Media type: E-Article
  • Title: De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway
  • Contributor: Asif, Maria; Kaygusuz, Emrah; Shinawi, Marwan; Nickelsen, Anna; Hsieh, Tzung-Chien; Wagle, Prerana; Budde, Birgit S.; Hochscherf, Jennifer; Abdullah, Uzma; Höning, Stefan; Nienberg, Christian; Lindenblatt, Dirk; Noegel, Angelika A.; Altmüller, Janine; Thiele, Holger; Motameny, Susanne; Fleischer, Nicole; Segal, Idan; Pais, Lynn; Tinschert, Sigrid; Samra, Nadra Nasser; Savatt, Juliann M.; Rudy, Natasha L.; De Luca, Chiara; [...]
  • Published: Elsevier BV, 2022
  • Published in: Human Genetics and Genomics Advances, 3 (2022) 3, Seite 100111
  • Language: English
  • DOI: 10.1016/j.xhgg.2022.100111
  • ISSN: 2666-2477
  • Origination:
  • Footnote:
  • Access State: Open Access