Journal
European Journal of Human Genetics
Publication Date
11-1-2023
Volume
31
Issue
11
First Page
1251
Last Page
1260
Document Type
Open Access Publication
DOI
10.1038/s41431-023-01445-2
Rights and Permissions
Oppermann, H., Marcos-Grañeda, E., Weiss, L.A. et al. CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology. Eur J Hum Genet 31, 1251–1260 (2023). https://doi.org/10.1038/s41431-023-01445-2 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
Oppermann, Henry; Gurnett, Christina A; and et al., "CUX1-related neurodevelopmental disorder: Deep insights into phenotype-genotype spectrum and underlying pathology." European Journal of Human Genetics. 31, 11. 1251 - 1260. (2023).
https://digitalcommons.wustl.edu/oa_4/3559
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.
