Simurda, Tomas <br/><br/>
Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia.  [electronic resource] 

 -  Seminars in thrombosis and hemostasis  Jun 2016 
 - 455-8 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>1098-9064 
<br/><br/><label>Standard No.: </label>10.1055/s-0036-1581104  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Afibrinogenemia--genetics<br/>Codon, Nonsense<br/>Fibrinogens, Abnormal--genetics<br/>Humans