Rare HFE variants are the most frequent cause of hemochromatosis in non-c282y homozygous patients with hemochromatosis

Heterozygous Mutations in BMP6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans

(2016) Raed Daher et al.   GASTROENTEROLOGY

Exploring genomic alteration in pediatric cancer using ProteinPaint

(2016) Xin Zhou et al.   NATURE GENETICS

Diagnostic Evaluation of Hereditary Hemochromatosis (HFE and Non-HFE)

(2014) Edouard Bardou-Jacquet et al.   HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA

Liver transplantation normalizes serum hepcidin level and cures iron metabolism alterations inHFEhemochromatosis

(2013) Edouard Bardou-Jacquet et al.   HEPATOLOGY

Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants

(2011) P. Aguilar-Martinez et al.   HAEMATOLOGICA

Diagnosis and management of hemochromatosis: 2011 Practice Guideline by the American Association for the Study of Liver Diseases

(2011) Bruce R. Bacon et al.   HEPATOLOGY

Hereditary Hemochromatosis: Pathogenesis, Diagnosis, and Treatment

(2010) Antonello Pietrangelo   GASTROENTEROLOGY

EASL clinical practice guidelines for HFE hemochromatosis

(2010)   JOURNAL OF HEPATOLOGY

Iron-Overload–Related Disease inHFEHereditary Hemochromatosis

(2008) Katrina J. Allen et al.   NEW ENGLAND JOURNAL OF MEDICINE