HEMOCHROMATOSIS, TYPE 3

Known as: HFE3, Hemochromatosis due to defect in transferrin receptor 2 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2000-2017
01220002017

Papers overview

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2017
2017
Type 3 haemochromatosis (HFE3) is a rare genetic iron overload disease which ultimately lead to compromised organs functioning… (More)
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2006
2006
Patients with porphyria cutanea tarda (PCT) reveal a susceptibility to reversible inactivation of hepatic uroporphyrinogen… (More)
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2004
2004
The influence of feeding hydrogenated fat (HF) or refined peanut oil (PO) diet and regular swimming exercise on hepatic and… (More)
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2001
2001
Hereditary hemochromatosis (HH) is a genetically heterogeneous disease. The HFE gene resides on chromosome 6 and its mutations… (More)
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Highly Cited
2000
Highly Cited
2000
Haemochromatosis is a common recessive disorder characterized by progressive iron overload, which may lead to severe clinical… (More)
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Review
2000
Review
2000
The application of molecular genetics to haemochromatosis and experimental mutagenesis in animals has transformed our capacity to… (More)
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