论文信息 - Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay - 字舞流文

Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay

P. Nurden | J. Oldenburg | I. Hainmann | A. Greinacher | A. Pavlova | A. Superti-Furga | U. Tacke | B. Strahm | B. Zieger | M. Bommer | F. Lanza | I. Bartsch | K. Sandrock | A. Busse | M. Barth