Search Results - Busse, A.

Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I by Vannier, Corinne (Author) , Behnisch, Wolfgang (Author) , Bartsch, I. (Author) , Sandrock, K. (Author) , Ertle, Florian (Author) , Schmidt, K. (Author) , Busse, A. (Author) , Superti-Furga, A. (Author) , Kulozik, Andreas (Author) , Santoso, S. (Author) , Zieger, Barbara (Author) ,

• Resolving-System, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext