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pubmed-article:16476869pubmed:abstractTextHemochromatosis in white subjects is mostly due to homozygosity for the common C282Y substitution in HFE. Although clinical symptoms are preventable by early detection of the genetic predisposition and prophylactic treatment, population screening is not currently advocated because of the discrepancy between the common mutation prevalence and apparently lower frequency of clinical disease. This study compared screening for hemochromatosis in subjects with or without a family history.lld:pubmed
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pubmed-article:16476869pubmed:articleTitleScreening for hemochromatosis in asymptomatic subjects with or without a family history.lld:pubmed
pubmed-article:16476869pubmed:affiliationCentre for the Advancement of Clinical Research, Royal Brisbane & Women's Hospital, Brisbane, Queensland 4029, Australia. Lawrie.Powell@qimr.edu.aulld:pubmed
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