Levy, N J <br/><br/>
Type II hereditary angioneurotic edema that may result from a single nucleotide change in the codon for alanine-436 in the C1 inhibitor gene.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Jan 1990 
 - 265-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.87.1.265  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alanine<br/>Amino Acid Sequence<br/>Angioedema--genetics<br/>Base Sequence<br/>Codon--genetics<br/>Complement C1 Inactivator Proteins--analysis<br/>DNA--blood<br/>Genes<br/>Humans<br/>Leukocytes--immunology<br/>Molecular Sequence Data<br/>Mutation<br/>Polymerase Chain Reaction<br/>RNA, Messenger--genetics