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October 15, 2012British Journal of HaematologyOpen Access

Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia

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Authors

SSSusan ShapiroUniversity of OxfordEPEmma PhillipsRoyal Marsden NHS Foundation TrustRMRichard A. ManningGuy's and St Thomas' NHS Foundation Trust

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Shapiro et al. (2012) studied this question.

synapsesocial.com/papers/6a96fb7861dfe9432d02099fhttps://doi.org/10.1111/bjh.12085
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Crystal Structure of Fragment Double-D from Human Fibrin with Two Different Bound Ligands,1998 · 164 citations
  2. 2The Sequence of Cleavage of Fibrinopeptides from Fibrinogen is Important for Protofibril Formation and Enhancement of Lateral Aggregation in Fibrin Clots1993 · 135 citations
  3. 3Familial Dysfibrinogenemia and Thrombophilia1995 · 340 citations