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Iranian hereditary hemochromatosis patients: Baseline characteristics, laboratory data and gene mutations
BACKGROUND: Hereditary hemochromatosis (HH) is the most common autosomal recessive disorder in white people, characterized by highly abnormal uptake of iron from the gastrointestinal tracts. Recently, mutation studies have focused to detect the genes responsible for HH. MATERIAL/METHODS: In this cro...
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
International Scientific Literature, Inc.
2012
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560564/ https://www.ncbi.nlm.nih.gov/pubmed/23018356 http://dx.doi.org/10.12659/MSM.883489 |