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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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| Publicado no: | J Clin Med Res |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elmer Press
2019
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| Assuntos: | |
| Acesso em linha: | 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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