Autosomal-dominant hemochrom-atosis is associated with a mutation in the ferroportin (SLC11A3) gene-Reference-Cited by-同舟云学术

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

Published:2001-08-15 Issue:4 Volume:108 Page:619-623
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Montosi Giuliana,Donovan Adriana,Totaro Angela,Garuti Cinzia,Pignatti Elisa,Cassanelli Stefano,Trenor Cameron C.,Gasparini Paolo,Andrews Nancy C.,Pietrangelo Antonello

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference18 articles.

1. Geography ofHFEC282Y and H63D Mutations

2. A novel MHC class I–like gene is mutated in patients with hereditary haemochromatosis

3. The Significance of the 187G (H63D) Mutation in Hemochromatosis

4. The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22

5. New mutations inactivating transferrin receptor 2 in hemochromatosis type 3

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1. Hepatic immune regulation and sex disparities;Nature Reviews Gastroenterology & Hepatology;2024-09-05

2. Hemochromatosis—How Not to Overlook and Properly Manage “Iron People”—A Review;Journal of Clinical Medicine;2024-06-23

3. Genetics of liver disease in adults;Hepatology Communications;2024-03-29

4. Hemocromatosis;Medicine - Programa de Formación Médica Continuada Acreditado;2024-03

5. Disorders of Iron Overload;MacSween's Pathology of the Liver;2024

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