Abstract
The gene for hemochromatosis was identified in 1996 and two mutations were found. Homozygosity for one of these, C282Y, is associated with hemochromatosis in a high percentage of patients. Genetic analysis of patient DNA is, therefore, a very useful tool to aid and confirm diagnosis and to screen asymptomatic relatives of patients to identify those at risk of developing this common, easily treated disease.
MeSH terms
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DNA Primers
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HLA Antigens / genetics*
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Hemochromatosis / genetics
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Hemochromatosis Protein
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Histocompatibility Antigens Class I / genetics*
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Humans
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Membrane Proteins*
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Mutation*
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Nucleic Acid Heteroduplexes
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Polymerase Chain Reaction / methods
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Polymorphism, Restriction Fragment Length
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Polymorphism, Single-Stranded Conformational
Substances
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DNA Primers
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HFE protein, human
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HLA Antigens
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Hemochromatosis Protein
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Histocompatibility Antigens Class I
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Membrane Proteins
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Nucleic Acid Heteroduplexes