7 results on '"Obser T"'
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2. Common large partial VWF gene deletion does not cause alloantibody formation in the Hungarian type 3 von Willebrand disease population
3. Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotype
4. Shear‐induced unfolding activates von Willebrand factor A2 domain for proteolysis
5. Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM-1VWD study
6. An Alu‐mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary
7. Genetic defects in von Willebrand disease type 3 in Indian and Greek patients
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