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Finally, the cross-sectional nature of the study limits the interpretation of the findings to only correlations
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The most common form of hereditary hemochromatosis (HH) is caused by mutations in the HFE, TFR1, hemojuvelin, hepcidin, or FPN genes
During the evolution process from prokaryotes into eukaryotes, the bacteria became mitochondria and shed most of their genetic material [96]
Biochem Pharmacol (2004) 68(6):10417
