A single F153Sβ3 mutation causes constitutive integrin αIIbβ3 activation in a variant form of Glanzmann thrombasthenia

por 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, Wilcox, David A.
Publicado 2023