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Hemochromatosis in a β‐thalassemia minor patient with H63D homozygous mutation: A case report
β‐thalassemia heterozygosity can cause significant iron overload when accompanied by HFE gene mutations and inappropriate iron supplementation.
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| Publicat a: | Clin Case Rep |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7752352/ https://ncbi.nlm.nih.gov/pubmed/33363736 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.3096 |
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