Lux, A <br/><br/>
Expression analysis of endoglin missense and truncation mutations: insights into protein structure and disease mechanisms.  [electronic resource] 

 -  Human molecular genetics  Mar 2000 
 - 745-55 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/9.5.745  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antigens, CD<br/>Base Sequence<br/>Cytoplasm--metabolism<br/>DNA Primers<br/>Dimerization<br/>Endoglin<br/>Exons<br/>Frameshift Mutation<br/>Glycosylation<br/>Humans<br/>Mutation, Missense<br/>Protein Conformation<br/>Receptors, Cell Surface<br/>Vascular Cell Adhesion Molecule-1--chemistry