Journal
Blood Advances
Publication Date
7-11-2023
Volume
7
Issue
13
First Page
3180
Last Page
3191
Document Type
Open Access Publication
DOI
10.1182/bloodadvances.2022009495
Rights and Permissions
Koukouritaki SB, Thinn AMM, Ashworth KJ, Fang J, Slater HS, Du LM, Nguyen HTT, Pillois X, Nurden AT, Ng CJ, Di Paola J, Zhu J, Wilcox DA. A single F153Sβ3 mutation causes constitutive integrin αIIbβ3 activation in a variant form of Glanzmann thrombasthenia. Blood Adv. 2023 Jul 11;7(13):3180-3191. doi: 10.1182/bloodadvances.2022009495. © 2023 by The American Society of Hematology. 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.
Recommended Citation
Koukouritaki, Sevasti B; Thinn, Aye Myat M; Ashworth, Katrina J; Fang, Juan; Slater, Haley S; Du, Lily M; Nguyen, Huong Thi Thu; Pillois, Xavier; Nurden, Alan T; Ng, Christopher J; Di Paola, Jorge; Zhu, Jieqing; and Wilcox, David A, "A single F153Sβ3 mutation causes constitutive integrin αIIbβ3 activation in a variant form of Glanzmann thrombasthenia." Blood Advances. 7, 13. 3180 - 3191. (2023).
https://digitalcommons.wustl.edu/oa_4/2203
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.
