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Journal of Hepatology, ISSN 0168-8278, 01/2019, Volume 70, Issue 1, pp. 118 - 125
Genetic hemochromatosis is mainly related to the homozygous p.Cys282Tyr (C282Y) mutation in the gene, which causes hepcidin deficiency. Its low penetrance... 
Phenotype | Tobacco | Genotype | Evolution | Alcohol | HFE hemochromatosis | BMI | FIBROSIS | IRON-OVERLOAD | HFE | HEPCIDIN | GASTROENTEROLOGY & HEPATOLOGY | Transferrin | Body weight | Liver | Ferritin | Tobacco smoking | Arthritis | Males | Risk factors | Cofactors | Genetic screening | Genetic factors | Diagnosis | Pancreas | Hemochromatosis | Diabetes mellitus | Fatigue | Homozygotes | Cirrhosis | Fibrosis | HFE protein | Diabetes | Females | Hepcidin | Smoking
Journal Article
European Radiology, ISSN 0938-7994, 5/2018, Volume 28, Issue 5, pp. 2022 - 2030
Journal Article
Journal Article
Journal Article
Journal Article
Endocrine, ISSN 1355-008X, 9/2017, Volume 57, Issue 3, pp. 504 - 511
Journal Article
Journal Article
Journal Article
Journal of Hepatology, ISSN 0168-8278, 2018, Volume 70, Issue 1, pp. 118 - 125
Genetic hemochromatosis is mainly related to the homozygous genotype for the HFE p.Cys282Tyr (C282Y) mutation leading to hepcidin deficiency. Its low... 
Life Sciences
Journal Article
European Journal of Applied Physiology, ISSN 1439-6319, 4/2012, Volume 112, Issue 4, pp. 1391 - 1397
Journal Article