Fredrikson, G N <br/><br/>
Molecular characterization of properdin deficiency type III: dysfunction produced by a single point mutation in exon 9 of the structural gene causing a tyrosine to aspartic acid interchange.  [electronic resource] 

 -  Journal of immunology (Baltimore, Md. : 1950)  Oct 1996 
 - 3666-71 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-1767 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Complement C3--metabolism<br/>Exons<br/>Genes<br/>Genes, Recessive<br/>Genetic Linkage<br/>Humans<br/>In Vitro Techniques<br/>Male<br/>Meningococcal Infections--genetics<br/>Molecular Sequence Data<br/>Oligopeptides--metabolism<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Properdin--deficiency<br/>Protein Binding<br/>Sequence Analysis<br/>X Chromosome--genetics