Wang, X <br/><br/>
Inherited human complement C5 deficiency. Nonsense mutations in exons 1 (Gln1 to Stop) and 36 (Arg1458 to Stop) and compound heterozygosity in three African-American families.  [electronic resource] 

 -  Journal of immunology (Baltimore, Md. : 1950)  May 1995 
 - 5464-71 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0022-1767 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Sequence<br/>Base Sequence<br/>Black People--genetics<br/>Complement C5--deficiency<br/>Exons<br/>Humans<br/>Immunologic Deficiency Syndromes--ethnology<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Black or African American