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HFE protein impact on iron metabolism
Hereditary hemochromatosis type 1 is an autosomal recessive disorder caused by HFE gene mutations, which is an iron homeostasis metabolism controlling co-factor. Adults with male predomination present with clinical symptoms derived by iron overload in organs. The phenotype expression is individual w...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Sciendo
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8522971/ https://www.ncbi.nlm.nih.gov/pubmed/28796976 http://dx.doi.org/10.34763/devperiodmed.20172102.8590 |