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March 1, 1995British Journal of Haematology

A novel candidate mutation (Arg611→ His) in type I‘platelet discordant’von Willebrand's disease with desmopressin‐induced thrombocytopenia

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Authors

GCGiancarlo CastamanJEJeroen EikenboomFRFrancesco Rodeghiero

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Castaman et al. (1995) studied this question.

synapsesocial.com/papers/6aa3f3ccfd19ae9969b154bchttps://doi.org/10.1111/j.1365-2141.1995.tb08383.x
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Also Consider

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

  1. 1A Revised Classification of von Willebrand Disease1994 · 593 citations
  2. 2Family studies and prenatal diagnosis in severe von Willebrand disease by polymerase chain reaction amplification of a variable number tandem repeat region of the von Willebrand factor gene1990 · 159 citations
  3. 3Heterogeneity of type I von Willebrand disease: evidence for a subgroup with an abnormal von Willebrand factor1985 · 185 citations
  4. 4Von Willebrand Disease: A Database of Point Mutations, Insertions, and Deletions1993 · 215 citations
  5. 5Structure of the gene for human von Willebrand factor1989 · 498 citations