Kluft, C <br/><br/>
Congenital deficiencies in alpha 2-antiplasmin.  [electronic resource] 

 -  La Ricerca in clinica e in laboratorio   
 - 507-13 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>0390-5748 
<br/><br/><label>Standard No.: </label>10.1007/BF02904878  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Binding Sites<br/>Blood Coagulation Disorders--congenital<br/>Fibrin--metabolism<br/>Fibrinolysin--metabolism<br/>Fibrinolysis<br/>Genetic Carrier Screening<br/>Homozygote<br/>Humans<br/>Lysine--metabolism<br/>Methods<br/>Plasminogen--metabolism<br/>alpha-2-Antiplasmin--analysis