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