Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleEnrichment of HFE mutations in Swedish patients with familial and sporadic form of porphyria cutanea tarda.AuthorsHarper, P.; Floderus, Y.; Holmström, P.; Eggertsen, C.; Cåfvels, M.AbstractPresents a letter to the editor about enrichment of HFE mutations in patients with sporadic form of porphyria cutanea tarda.SubjectsLETTERS to the editor; GENETIC mutationPublicationJournal of Internal Medicine, 2004, Vol 255, Issue 6, p684ISSN0954-6820Publication typeLetterDOI10.1111/j.1365-2796.2004.01309.x