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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...
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| Pubblicato in: | J Clin Med Res |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Elmer Press
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6522237/ https://ncbi.nlm.nih.gov/pubmed/31143309 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14740/jocmr3816 |
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