Characterization of the mutation spectrum in a Pakistani cohort of type 3 von Willebrand disease

Type-3 von Willebrand disease in India-Clinical spectrum and molecular profile

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The spectrum of mutations in Southern Spanish patients with von Willebrand disease

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Mutations in the D1 domain of von Willebrand factor impair their propeptide-dependent multimerization, intracellular trafficking and secretion

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The I-TASSER Suite: protein structure and function prediction

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YASARA View—molecular graphics for all devices—from smartphones to workstations

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Highly reinforced structure of a C-terminal dimerization domain in von Willebrand factor

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MutationTaster2: mutation prediction for the deep-sequencing age

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Genetic Heterogeneity in a Large Cohort of Indian Type 3 von Willebrand Disease Patients

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Alloantibodies in von Willebrand disease

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The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles

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Phenotypic and molecular characterisation of type 3 von Willebrand disease in a cohort of Indian patients

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Sequence and structure relationships within von Willebrand factor

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von Willebrand factor: the old, the new and the unknown

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Predicting the Functional Effect of Amino Acid Substitutions and Indels

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Implications for collagen I chain registry from the structure of the collagen von Willebrand factor A3 domain complex

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Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients

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The pathophysiology of von Willebrand disease: therapeutic implications

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von Willebrand disease

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von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional protein

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The genetic basis of von Willebrand disease

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A method and server for predicting damaging missense mutations

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The mutation spectrum associated with type 3 von Willebrand disease in a cohort of patients from the North West of England

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Genetic defects in von Willebrand disease type 3 in Indian and Greek patients

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Expression studies of missense mutations p.D141Y, p.C275S located in the propeptide of von Willebrand factor in patients with type 3 von Willebrand disease

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