Ferroportin disease: pathogenesis, diagnosis and treatment

Ferroportin Disease (FD) is an autosomal dominant hereditary iron loading disorder associated with heterozygote mutations of the ferroportin-1 (FPN) gene. It represents one of the commonest causes of genetic hyperferritinemia, regardless of ethnicity. FPN1 transfers iron from the intestine, macropha...

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Detalles Bibliográficos
Autor principal: Pietrangelo, Antonello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ferrata Storti Foundation 2017
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709096/
https://www.ncbi.nlm.nih.gov/pubmed/29101207
http://dx.doi.org/10.3324/haematol.2017.170720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5709096/
https://www.ncbi.nlm.nih.gov/pubmed/29101207
http://dx.doi.org/10.3324/haematol.2017.170720

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