Vu, D <br/><br/>
Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion.  [electronic resource] 

 -  Journal of medical genetics  Sep 2005 
 - e57 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.2005.033530  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Afibrinogenemia--blood<br/>Amino Acid Sequence<br/>Animals<br/>COS Cells<br/>Chlorocebus aethiops--metabolism<br/>Crystallography, X-Ray<br/>Exons<br/>Female<br/>Fibrinogen--chemistry<br/>Heterozygote<br/>Humans<br/>Models, Molecular<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Protein Structure, Tertiary<br/>Sequence Alignment<br/>Slovakia<br/>Transfection