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...

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Detalles Bibliográficos
Autores principales: Raszeja-Wyszomirska, Joanna, Caleffi, Angela, Milkiewicz, Piotr, Pietrangelo, Antonello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2014
Materias:
Case Report
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

Internet

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

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