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May 1, 1999British Journal of Haematology

Identification and characterization of a novel mutation in von Willebrand factor causing type 2B von Willebrand's disease

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Authors

DFDavid A. FaceyEFEmmanuel J. FavaloroJKJerry Koutts

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Facey et al. (1999) studied this question.

synapsesocial.com/papers/6a95c31bb3a30ccf5d319685https://doi.org/10.1111/j.1365-2141.1999.01358.x
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Unique interactions of asialo von Willebrand factor with platelets in platelet-type von Willebrand disease1987 · 18 citations
  2. 2Identification of aspartic acid 514 through glutamic acid 542 as a glycoprotein Ib-IX complex receptor recognition sequence in von Willebrand factor. Mechanism of modulation of von Willebrand factor by ristocetin and botrocetin1992 · 107 citations
  3. 3Von Willebrand Disease: A Database of Point Mutations, Insertions, and Deletions1993 · 215 citations
  4. 4Localization and characterization of a heparin binding domain peptide of human von Willebrand factor.1992 · 172 citations
  5. 5Type IIB von Willebrand's disease: gene mutations and clinical presentation in nine families from Denmark, Germany and Sweden1992 · 22 citations