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Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene

Hemochromatosis is a progressive iron overload disorder that is prevalent among individuals of European descent. It is usually inherited in an autosomal-recessive pattern and associated with missense mutations in HFE, an atypical major histocompatibility class I gene. Recently, we described a large...

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Autors principals: Montosi, Giuliana, Donovan, Adriana, Totaro, Angela, Garuti, Cinzia, Pignatti, Elisa, Cassanelli, Stefano, Trenor, Cameron C., Gasparini, Paolo, Andrews, Nancy C., Pietrangelo, Antonello
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2001
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC209405/
https://ncbi.nlm.nih.gov/pubmed/11518736
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