HFE H63D gene mutation
The HFE H63D is a single-nucleotide polymorphism in the HFE gene (c.187C>G, rs1799945), which results in the substitution of an aspartic acid for a histidine at amino acid position 63 of the HPE protein (p.His63Asp). HFE participates in the regulation of iron absorption.
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HFE H63D gene mutation
The HFE H63D is a single-nucleotide polymorphism in the HFE gene (c.187C>G, rs1799945), which results in the substitution of an aspartic acid for a histidine at amino acid position 63 of the HPE protein (p.His63Asp). HFE participates in the regulation of iron absorption.
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The HFE H63D is a single-nucle ...... and peripheral artery disease.
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The HFE H63D is a single-nucle ...... regulation of iron absorption.
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HFE H63D gene mutation
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