Journal
Cell Reports
Publication Date
11-10-2023
Volume
42
Issue
11
First Page
113411
Document Type
Open Access Publication
DOI
10.1016/j.celrep.2023.113411
Rights and Permissions
Beard DC, Zhang X, Wu DY, Martin JR, Erickson A, Boua JV, Hamagami N, Swift RG, McCullough KB, Ge X, Bell-Hensley A, Zheng H, Palmer CW, Fuhler NA, Lawrence AB, Hill CA, Papouin T, Noguchi KK, McAlinden A, Garbow JR, Dougherty JD, Maloney SE, Gabel HW. Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficits. Cell Rep. 2023 Nov 10;42(11):113411. doi: 10.1016/j.celrep.2023.113411. Copyright 2023 The Authors. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Recommended Citation
Beard, Diana C; Zhang, Xiyun; Wu, Dennis Y; Martin, Jenna R; Erickson, Alyssa; Boua, Jane Valeriane; Hamagami, Nicole; Swift, Raylynn G; McCullough, Katherine B; Ge, Xia; Bell-Hensley, Austin; Zheng, Hongjun; Palmer, Cory W; Fuhler, Nicole A; Papouin, Thomas; Noguchi, Kevin K; McAlinden, Audrey; Garbow, Joel R; Dougherty, Joseph D; Maloney, Susan E; Gabel, Harrison W; and et al., "Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficits." Cell Reports. 42, 11. 113411 (2023).
https://digitalcommons.wustl.edu/oa_4/2608
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.
