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Polycythemia in Patients With Hereditary Hemochromatosis: Real or Myth?
BACKGROUND: Hereditary hemochromatosis (HH) is an autosomal recessive disorder affecting iron metabolism, resulting in iron accumulation in tissue parenchymal cells. Missense mutations result in homozygosity or heterozygosity for substitutions in the HFE gene, with the most common being C282Y and H6...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Elmer Press
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6522237/ https://www.ncbi.nlm.nih.gov/pubmed/31143309 http://dx.doi.org/10.14740/jocmr3816 |