Anderson, P M <br/><br/>
Characterization of the porphobilinogen deaminase deficiency in acute intermittent porphyria. Immunologic evidence for heterogeneity of the genetic defect.  [electronic resource] 

 -  The Journal of clinical investigation  Jul 1981 
 - 1-12 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>0021-9738 
<br/><br/><label>Standard No.: </label>10.1172/jci110223  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Ammonia-Lyases--deficiency<br/>Antibodies<br/>Cross Reactions<br/>Erythrocytes--enzymology<br/>Genes<br/>Heterozygote<br/>Humans<br/>Mutation<br/>Porphyria, Acute Intermittent<br/>Porphyrias--enzymology