Sex and Acquired Cofactors Determine Phenotypes of Ferroportin Disease-Reference-Cited by-同舟云学术

Sex and Acquired Cofactors Determine Phenotypes of Ferroportin Disease

Published:2011-04 Issue:4 Volume:140 Page:1199-1207.e2
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Le Lan Caroline,Mosser Annick,Ropert Martine,Detivaud Lénaïck,Loustaud–Ratti Véronique,Vital–Durand Denis,Roget Laurent,Bardou–Jacquet Edouard,Turlin Bruno,David Véronique,Loréal Olivier,Deugnier Yves,Brissot Pierre,Jouanolle Anne–Marie

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference41 articles.

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2. A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis;Njajou;Nat Genet,2001

3. The ferroportin disease;Pietrangelo;Blood Cells Mol Dis,2004

4. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization;Nemeth;Science,2004

5. Autosomal dominant iron overload due to a novel mutation of ferroportin1 associated with parenchymal iron loading and cirrhosis;Wallace;J Hepatol,2004

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