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Blood|March 21, 1998
Type 2M von Willebrand disease: F606I and I662F mutations in the glycoprotein Ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to plateletsC A Hillery, D J Mancuso, J Evan Sadler, et al.Pageof 2