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Introduction
Type 3 von Willebrand disease (VWD) is the rare and most severe form of VWD which results from a near‐complete deficiency of the von Willebrand factor (VWF). This study evaluates in detail the molecular pathology of type‐3 VWD in India. One hundred and two patients from 90 families were evaluated.
Patients and methods
Phenotypic data, including bleeding scores (BS), were documented...