Hua, B <br/><br/>
Coexisting congenital dysfibrinogenemia with a novel mutation in fibrinogen γ chain (γ322 Phe→Ile, Fibrinogen Beijing) and haemophilia B in a family.  [electronic resource] 

 -  Haemophilia : the official journal of the World Federation of Hemophilia  Nov 2015 
 - 846-51 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2516 
<br/><br/><label>Standard No.: </label>10.1111/hae.12712  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Afibrinogenemia--complications<br/>Blood Coagulation Tests<br/>DNA Mutational Analysis<br/>Female<br/>Fibrinogen--chemistry<br/>Fibrinolysis<br/>Hemophilia B--complications<br/>Humans<br/>Male<br/>Mutation<br/>Pedigree<br/>Peptide Fragments--chemistry<br/>Protein Multimerization<br/>Protein Structure, Quaternary