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Frequency of Two Common HFE Gene Mutations (C282Y and H63D) in a Group of Iranian Patients With Cryptogenic Cirrhosis
BACKGROUND: The human HFE gene (a key component of iron homeostasis in humans) is involved in hereditary hemochromatosis, a common autosomal recessive genetic disorder that is characterized by excessive intestinal iron absorption and progressive iron overload. OBJECTIVES: In this study, we assessed...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Kowsar
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3269056/ https://ncbi.nlm.nih.gov/pubmed/22308152 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5812/kowsar.1735143x.781 |
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