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Ferroportin-related haemochromatosis associated with novel Y64H mutation of the SCL40A1 gene
In this paper we described the first Polish patient with ferroportin disease. Hereditary haemochromatosis (HH) is a condition associated with universal iron overload, and it is divided into four types, according to the Online Mendelian Inheritance in Man (OMIM) database. Ferroportin disease represen...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Termedia Publishing House
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4223120/ https://www.ncbi.nlm.nih.gov/pubmed/25396007 http://dx.doi.org/10.5114/pg.2014.46167 |