Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report
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DOI: 10.1186/s13256-020-02428-3
Abstract: Hereditary hemochromatosis is an inherited disorder of iron metabolism, characterized by excessive iron deposition in major organs of the body, leading to multi-organ dysfunction. It is a genetically heterogeneous disease caused by mutations in one… read more here.
Keywords: h63d mutation; gene; hereditary hemochromatosis; mutation ... See more keywords