Kotmayer, L., Oak, N., Halyko, M. et al. (10 more authors) (2026) Somatic UBA1 mutations in pediatric MDS/AML: first cases suggest distinct pathogenesis from adult VEXAS syndrome. Blood Neoplasia, 3 (3). 100228. ISSN: 2950-3280
Abstract
We report pediatric myeloid neoplasms with secondary somatic UBA1 mutations: one with somatic NRAS and UBA1_S56F subclone, another with germline RUNX1 disorder and somatic SH2B3 and UBA1_M41L clones. No UBA1 mutations were found among 834 pediatric AML cases.
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| Item Type: | Article |
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| Authors/Creators: |
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| Copyright, Publisher and Additional Information: | This article is protected by copyright. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. |
| Dates: |
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| Institution: | The University of Leeds |
| Academic Units: | The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Institute of Rheumatology & Musculoskeletal Medicine (LIRMM) (Leeds) > Inflammatory Arthritis (Leeds) |
| Date Deposited: | 17 Jul 2026 15:57 |
| Last Modified: | 17 Jul 2026 15:57 |
| Published Version: | https://www.sciencedirect.com/science/article/pii/... |
| Status: | Published |
| Publisher: | Elsevier |
| Identification Number: | 10.1016/j.bneo.2026.100228 |
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:243254 |
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