Hussain, S P <br/><br/>
Increased p53 mutation load in nontumorous human liver of wilson disease and hemochromatosis: oxyradical overload diseases.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Nov 2000 
 - 12770-5 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.220416097  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aldehydes--pharmacology<br/>Animals<br/>Cell Line<br/>Copper--metabolism<br/>Free Radicals<br/>Genes, MHC Class I<br/>HLA Antigens--genetics<br/>Hemochromatosis--genetics<br/>Hemochromatosis Protein<br/>Hepatolenticular Degeneration--genetics<br/>Histocompatibility Antigens Class I--genetics<br/>Humans<br/>Iron--metabolism<br/>Liver--metabolism<br/>Membrane Proteins<br/>Mutagenesis--drug effects<br/>Mutation<br/>Nitric Oxide Synthase--biosynthesis<br/>Nitric Oxide Synthase Type II<br/>Rabbits<br/>Tumor Suppressor Protein p53--genetics