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A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

Nature Genetics · 1996 · Vol. 13(4) · pp. 399–408

Iron Metabolism and Disorders Hemoglobinopathies and Related Disorders Complement system in diseasesBiologyGeneticsMajor histocompatibility complexHaplotypeLinkage disequilibriumMissense mutationGeneMHC class IGenetic linkageMutation

MeSH terms

Hemochromatosis ProteinAllelesAmino Acid SequenceBase SequenceChromosomes, Human, Pair 6Cloning, MolecularCysteineBiological EvolutionGenes, MHC Class IGenetic MarkersHaplotypesHemochromatosisHLA AntigensHumansMajor Histocompatibility Complex

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