protein, also known as the HFE protein (High FE2+), is a transmembrane protein that in humans is encoded by the HFE gene. The HFE gene is located on short arm...

The HFE H63D is a single-nucleotide polymorphism in the HFE gene (c.187C>G, rs1799945), which results in the substitution of a histidine for an aspartic...

5, all caused by mutated genes. Hereditary hemochromatosis type 1 is the most frequent, and unique related to the HFE gene. It is most common among those...

the C282Y mutation on the HFE gene, and 1% having the condition. The overwhelming majority depend on mutations of the HFE gene discovered in 1996, but since...

HFE may refer to: HFE (gene), a gene that encodes the Human hemochromatosis protein Hello from Earth, an interstellar radio message Hidden Field Equations...

hemochromatosis gene region". Hum Genet 102: 517–25. Milman N, Pedersen P (2003). "Evidence that the Cys282Tyr mutation of the HFE gene originated from...

HFE gene. A 2006 clinical, biochemical and mutational study of eight Swiss variegate porphyria patients and their families found four novel PPOX gene...

The HFE gene provides instructions for producing a protein that is located on the surface of cells, primarily liver and intestinal cells. The HFE protein...

the signs and symptoms of porphyria cutanea tarda.[citation needed] The HFE gene makes a protein that helps cells regulate the absorption of iron from the...

PNPLA3 gene, and was compound heterozygous for two type-1 classical hereditary hemochromatosis mutations, rs1799945 and rs1800562, in the HFE gene. Beethoven’s...