Wypasek, Ewa <br/><br/>
Heerlen polymorphism associated with type III protein S deficiency and factor V Leiden mutation in a Polish patient with deep vein thrombosis.  [electronic resource] 

 -  Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis  Jan 2014 
 - 84-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1473-5733 
<br/><br/><label>Standard No.: </label>10.1097/MBC.0b013e328365032c  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blood Proteins--genetics<br/>Factor V--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Poland<br/>Polymorphism, Genetic<br/>Protein S<br/>Protein S Deficiency--blood<br/>Venous Thrombosis--blood