A single F153Sβ3 mutation causes constitutive integrin αIIbβ3 activation in a variant form of Glanzmann thrombasthenia.
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.
Koukouritaki SB, et al. Among authors: zhu j.
Blood Adv. 2023 Jul 11;7(13):3180-3191. doi: 10.1182/bloodadvances.2022009495.
Blood Adv. 2023.
PMID: 36884296
Free PMC article.