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Naturally variant autosomal and sex-linked loci determine the severity of iron overload in β(2)-microglobulin-deficient mice
Hereditary hemochromatosis (HH) is a common chronic human genetic disorder whose hallmark is systemic iron overload. Homozygosity for a mutation in the MHC class I heavy chain paralogue gene HFE has been found to be a primary cause of HH. However, many individuals homozygous for the defective allele...
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