de Villiers, J N <br/><br/>
High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa.  [electronic resource] 

 -  South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde  Mar 1999 
 - 279-82 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0256-9574 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alleles<br/>Female<br/>Genetic Testing--methods<br/>Genotype<br/>Hemochromatosis--diagnosis<br/>Homozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>South Africa