Fitches, A C <br/><br/>
Impaired cotranslational processing as a mechanism for type I antithrombin deficiency.  [electronic resource] 

 -  Blood  Dec 1998 
 - 4671-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amino Acid Substitution--genetics<br/>Animals<br/>Antithrombins--chemistry<br/>COS Cells<br/>Cell-Free System<br/>DNA Mutational Analysis<br/>Dogs<br/>Female<br/>Gene Expression<br/>Glycosylation<br/>Humans<br/>Leucine--genetics<br/>Microsomes--metabolism<br/>Pancreas--metabolism<br/>Point Mutation--genetics<br/>Proline--genetics<br/>Protein Processing, Post-Translational<br/>Protein Sorting Signals--genetics<br/>Transfection