Recurrent pulmonary embolism associated with deep venous thrombosis diagnosed as protein s deficiency owing to a novel mutation in PROS1
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference26 articles.
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3. Pros1 analysis in 87 pedigrees with hereditary protein s deficiency demonstrates striking genotype-phenotype associations;Ten Kate;Hum Mutat,2008
4. Protein S binds to and inhibits factor Xa;Heeb;Proc Natl Acad Sci U S A,1994
5. The interaction of protein S with the phospholipid surface is essential for the activated protein C-independent activity of protein S;van Wijnen;Thromb Haemost,1996
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