HFE gene

Known as: HLAH, hemochromatosis, HLA-H 
This gene plays a role in the modulation of iron transport.
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
BACKGROUND & AIMS Mutations in the hemochromatosis gene (HFE) (C282Y and H63D) lead to parenchymal iron accumulation… (More)
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Review
2007
Review
2007
UNLABELLED More than 70% of alcohol is consumed by 10% of the population in the United States. Implicit in this statistic is that… (More)
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Highly Cited
2003
Highly Cited
2003
BACKGROUND & AIMS Mild to moderate hepatic iron loading is common in patients with chronic hepatitis C. We sought to determine… (More)
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2002
2002
Hereditary hemochromatosis is most commonly caused by homozygosity for a point mutation (C282Y) in the human hemochromatosis gene… (More)
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Highly Cited
2001
Highly Cited
2001
Hereditary hemochromatosis (HH) is a common disorder of iron metabolism caused by mutation in HFE, a gene encoding an MHC class I… (More)
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Highly Cited
2000
Highly Cited
2000
Hereditary hemochromatosis (HH) is a prevalent human disease caused by a mutation in HFE, which encodes an atypical HLA class I… (More)
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Highly Cited
1999
Highly Cited
1999
The puzzling linkage between genetic hemochromatosis and histocompatibility loci became even more so when the gene involved, HFE… (More)
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Highly Cited
1999
Highly Cited
1999
Background-Homozygosity for a relatively common Cys282Tyr mutation of the human hemochromatosis-associated (HFE) gene was… (More)
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1992
1992
The hypothesized relationship betWfttl the relati~e streftlth of sexual seltdklll and life-history 5tr8tt1it5 is reexamined. The… (More)
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1991
1991
PURPOSE To investigate the changing modes of clinical presentation and diagnosis in 93 patients with familial hemochromatosis and… (More)
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