Juvenile Hemochromatosis: A Case Report and Review of the Literature
Juvenile hemochromatosis (JH), type 2A hemochromatosis, is a rare autosomal recessive disorder of systemic iron overload due to homozygous mutations of <i>HJV</i> (<i>HFE2</i>), which encodes hemojuvelin, an essential regulator of the hepcidin expression, causing liver fibros...
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Format: | Book |
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MDPI AG,
2020-08-01T00:00:00Z.
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A1234.567 |
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