Schilsky, M L <br/><br/>
Wilson disease: genetic basis of copper toxicity and natural history.  [electronic resource] 

 -  Seminars in liver disease  Feb 1996 
 - 83-95 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>0272-8087 
<br/><br/><label>Standard No.: </label>10.1055/s-2007-1007221  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Carrier Proteins--genetics<br/>Cation Transport Proteins<br/>Chelating Agents--therapeutic use<br/>Chelation Therapy<br/>Chromosome Mapping<br/>Copper--adverse effects<br/>Copper-Transporting ATPases<br/>Environment<br/>Genetic Therapy<br/>Genome, Human<br/>Hepatitis--surgery<br/>Hepatolenticular Degeneration--genetics<br/>Humans<br/>Liver Transplantation<br/>Molybdenum--therapeutic use<br/>Mutation--genetics<br/>Penicillamine--therapeutic use<br/>Risk Factors<br/>Trientine--therapeutic use<br/>Zinc--therapeutic use