Stuart, K A <br/><br/>
The C282Y mutation in the haemochromatosis gene (HFE) and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients.  [electronic resource] 

 -  Journal of hepatology  Mar 1998 
 - 404-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0168-8278 
<br/><br/><label>Standard No.: </label>10.1016/s0168-8278(98)80313-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Australia<br/>Female<br/>Ferritins--blood<br/>Gene Dosage<br/>Gene Frequency--genetics<br/>Hemochromatosis--genetics<br/>Hepacivirus--immunology<br/>Hepatitis C--genetics<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Immunoglobulin G--analysis<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Porphyria Cutanea Tarda--genetics<br/>Transferrin--analysis