Ferroportin disease: A novel SLC40A1 mutation

Dig Liver Dis. 2020 Jun;52(6):688-690. doi: 10.1016/j.dld.2020.03.013. Epub 2020 Apr 29.

¹ University of Milano-Bicocca - Department of Medicine and Surgery, Monza, Italy.
² Medical Genetics - ASST-Monza, S.Gerardo Hospital, Monza, Italy.
³ Centre for Rare Diseases - Disorders of Iron Metabolism - ASST-Monza, EuroBloodNet Referral Centre, S.Gerardo Hospital, Monza, Italy.
⁴ University of Milano-Bicocca - Department of Medicine and Surgery, Monza, Italy; Medical Genetics - ASST-Monza, S.Gerardo Hospital, Monza, Italy; Centre for Rare Diseases - Disorders of Iron Metabolism - ASST-Monza, EuroBloodNet Referral Centre, S.Gerardo Hospital, Monza, Italy. Electronic address: alberto.piperno@unimb.it.

No abstract available

Keywords: Ferritin; Ferroportin; Hereditary hemochromatosis; Iron overload.

Publication types