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6. HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France. Dereure O, Aguilar-Martinez P, Bessis D, Perney P, Vallat C, Guillot B, Blanc F, Guilhou JJ. Br J Dermatol; 2001 Mar; 144(3):533-9. PubMed ID: 11260010 [Abstract] [Full Text] [Related]
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16. Uroporphyria in Hfe mutant mice given 5-aminolevulinate: a new model of Fe-mediated porphyria cutanea tarda. Sinclair PR, Gorman N, Walton HS, Bement WJ, Sinclair JF, Gerhard GS, Szakacs JG, Andrews NC, Levy JE. Hepatology; 2001 Feb 31; 33(2):406-12. PubMed ID: 11172342 [Abstract] [Full Text] [Related]
17. High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda. Sampietro M, Piperno A, Lupica L, Arosio C, Vergani A, Corbetta N, Malosio I, Mattioli M, Fracanzani AL, Cappellini MD, Fiorelli G, Fargion S. Hepatology; 1998 Jan 31; 27(1):181-4. PubMed ID: 9425935 [Abstract] [Full Text] [Related]
19. The frequency of hemochromatosis-associated alleles is increased in British patients with sporadic porphyria cutanea tarda. Roberts AG, Whatley SD, Nicklin S, Worwood M, Pointon JJ, Stone C, Elder GH. Hepatology; 1997 Jan 31; 25(1):159-61. PubMed ID: 8985283 [Abstract] [Full Text] [Related]