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Anderson, Eric N. ; Drukewitz, Stephan ; Kour, Sukhleen ; Chimata, Anuradha V. ; Rajan, Deepa S. ; Schönnagel, Senta ; Stals, Karen L. ; Donnelly, Deirdre ; O'Sullivan, Siobhan ; Mantovani, John F. ; Tan, Tiong Y. ; Stark, Zornitza ; Zacher, Pia ; Chatron, Nicolas ; Monin, Pauline ; Drunat, Severine ; Vial, Yoann ; Latypova, Xenia ; Levy, Jonathan ; Verloes, Alain ; Carter, Jennefer N. ; Bonner, Devon E. ; Shankar, Suma P. ; Bernstein, Jonathan A. ; Cohen, Julie S. ; Comi, Anne ; Carere, Deanna Alexis ; Dyer, Lisa M. ; Mullegama, Sureni V. ; Sanchez-Lara, Pedro A. ; Grand, Katheryn ; Kim, Hyung-Goo ; Ben-Mahmoud, Afif ; Gospe, Sidney M. ; Belles, Rebecca S. ; Bellus, Gary ; Lichtenbelt, Klaske D. ; Oegema, Renske ; Rauch, Anita ; Ivanovski, Ivan ; Mau-Them, Frederic Tran ; Garde, Aurore ; Rabin, Rachel ; Pappas, John ; Bley, Annette E. ; Bredow, Janna ; Wagner, Timo ; Decker, Eva ; Bergmann, Carsten ; Domenach, Louis ; Margot, Henri ; Lemke, Johannes R. ; Abou Jamra, Rami ; Hentschel, Julia ; Mefford, Heather ; Singh, Amit ; Pandey, Udai Bhan ; Platzer, Konrad (2026).
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder
PMID: 41468891, DOI: 10.1016/j.ajhg.2025.12.004, S2CID: 277492716.
American Journal of Human Genetics, 113(1), 100–116. 2026, January 8.