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Clinical impact of heterozygosity for the C282Y and H63D mutation of the hemochromatosis (HFE) gene in chloroquine treated patients with porphyria cutanea tarda (PCT) in Germany

✍ Scribed by Stoelzel, Ulrich; Tannapfel, Andrea; Schuppan, Detlef; Richter, Matthias; Keim, Volker; Doss, Manfred O.; Melz, Steffi; Koestler, Erich


Book ID
124122265
Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
178 KB
Volume
120
Category
Article
ISSN
0016-5085

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C282Y and H63D mutations in the HFE gene
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Viral genotyping was performed in 61 patients with untreated chronic hepatitis C using the Inno-Lipa HCV II assay (Innogenetics, Zwijnaarde, Belgium). Steatosis was graded as previously reported. 1 The association between viral genotype and steatosis was tested using the Pearson' s 2 statistic and t