Associated Papers
Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort.
Hampshire DJ et al.
Haematologica, 2010
Prevalence and spectrum of von Willebrand disease from western India.
Trasi S et al.
The Indian Journal of Medical Research, 2005
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