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A case report of hereditary hemochromatosis caused by mutation of SLC40A1 gene
RATIONALE: Hereditary hemochromatosis (HH) is a frequent autosomal recessive disease. The pathogenesis of disease is excessive intestinal absorption of dietary iron, resulting in pathologically high iron storage in tissues and organs. As a systemic disease, it has several manifestations including ci...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Wolters Kluwer Health
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6946363/ https://www.ncbi.nlm.nih.gov/pubmed/31689754 http://dx.doi.org/10.1097/MD.0000000000017526 |