De novo variants in KDM2A cause a syndromic neurodevelopmental disorder

Zurich Open Repository and Archive (University of Zurich) 2026 Open access

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Authors: Eric Nathaniel Anderson, Stephan Drukewitz, Sukhleen Kour, Anuradha Venkatakrishnan Chimata, Deepa Soundara Rajan, Senta Schönnagel, Karen Lucy Stals, Deirdre Donnelly, O'Sullivan, Siobhan, John F. Mantovani, Tiong Yang Tan, Zornitza Stark
+21 more Pia Zacher, Nicolas Chatron, Pauline Monin, Séverine Drunat, Yoann Vial, Xénia Latypova, Jonathan Lévy, Alain Verloès, Jennefer N. Carter, Devon E. Bonner, Suma P. Shankar, Jonathan Adam Bernstein, Julie S. Cohen, Anne M. Comi, Deanna Alexis Carere, Lisa M. Dyer, Sureni V. Mullegama, Pedro Alfonso Sanchez-Lara, et al, Anita M. Rauch, Ivan P. Ivanovski
DOI: 10.5167/uzh-282551
Cited by: 0

Fields of Study & Subjects

Genetics and Neurodevelopmental Disorders Genomics and Rare Diseases Epigenetics and DNA Methylation

Publication details

Journal / source
Zurich Open Repository and Archive (University of Zurich)
Publication date
8 January 2026
Language
EN