Journal
European Journal of Human Genetics
Publication Date
4-1-2026
Volume
34
Issue
4
First Page
554
Last Page
564
Document Type
Open Access Publication
DOI
10.1038/s41431-026-02017-w
Rights and Permissions
Jost, C., Busa, T., Wegner, D. et al. De novo heterozygous variants of the RSF1 gene are responsible for a syndromic neurodevelopmental disorder. Eur J Hum Genet 34, 554–564 (2026). https://doi.org/10.1038/s41431-026-02017-w This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
Recommended Citation
Jost, Céline; Wegner, Daniel; Shinawi, Marwan; Sisco, Kathleen; J Paul, Alexander; and et al., "De novo heterozygous variants of the RSF1 gene are responsible for a syndromic neurodevelopmental disorder." European Journal of Human Genetics. 34, 4. 554 - 564. (2026).
https://digitalcommons.wustl.edu/oa_4/7562
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.
