Journal
Genetics in Medicine
Publication Date
8-1-2020
Volume
22
Issue
8
First Page
1413
Last Page
1417
Document Type
Open Access Publication
DOI
10.1038/s41436-020-0815-4
Rights and Permissions
Singh S, Gupta A, Zech M, Sigafoos AN, Clark KJ, Dincer Y, Wagner M, Humberson JB, Green S, van Gassen K, Brandt T, Schnur RE, Millan F, Si Y, Mall V, Winkelmann J, Gavrilova RH, Klee EW, Engleman K, Safina NP, Slaugh R, Bryant EM, Tan WH, Granadillo J, Misra SN, Schaefer GB, Towner S, Brilstra EH, Koeleman BPC. De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy. Genet Med. 2020 Aug;22(8):1413-1417. doi: 10.1038/s41436-020-0815-4 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/ by/4.0/.
Recommended Citation
Singh, Sakshi; Slaugh, Rachel; Granadillo, Jorge; and et al., "De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy." Genetics in Medicine. 22, 8. 1413 - 1417. (2020).
https://digitalcommons.wustl.edu/oa_4/529
Supplemental Material
