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Distinct disease mutations in DNMT3A result in a spectrum of behavioral, epigenetic, and transcriptional deficits.
Beard DC, Zhang X, Wu DY, Martin JR, Hamagami N, Swift RG, McCullough KB, Ge X, Bell-Hensley A, Zheng H, Lawrence AB, Hill CA, Papouin T, McAlinden A, Garbow JR, Dougherty JD, Maloney SE, Gabel HW. Beard DC, et al. Among authors: maloney se. bioRxiv [Preprint]. 2023 Feb 27:2023.02.27.530041. doi: 10.1101/2023.02.27.530041. bioRxiv. 2023. PMID: 36909558 Free PMC article. Updated. Preprint.
Characterization of a Mouse Model of Börjeson-Forssman-Lehmann Syndrome.
Cheng C, Deng PY, Ikeuchi Y, Yuede C, Li D, Rensing N, Huang J, Baldridge D, Maloney SE, Dougherty JD, Constantino J, Jahani-Asl A, Wong M, Wozniak DF, Wang T, Klyachko VA, Bonni A. Cheng C, et al. Among authors: maloney se. Cell Rep. 2018 Nov 6;25(6):1404-1414.e6. doi: 10.1016/j.celrep.2018.10.043. Cell Rep. 2018. PMID: 30403997 Free PMC article.
68 results