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Springer Publishing Company

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A Rare Case of a Patient Heterozygous for the Hemochromatosis Mutation C282Y and Homozygous for H63D

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Frequency of the C282Y Mutation of Hemochromatosis in Five French Populations

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Pearson syndrome in an infant heterozygous for C282Y allele of HFE gene

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Celtic Origin of the C282Y Mutation of Hemochromatosis

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