Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis-Reference-Cited by-同舟云学术

Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis

Published:2012-10 Issue:1 Volume:508 Page:15-20
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

del-Castillo-Rueda Alejandro,Moreno-Carralero María-Isabel,Cuadrado-Grande Nuria,Álvarez-Sala-Walther Luis-Antonio,Enríquez-de-Salamanca Rafael,Méndez Manuel,Morán-Jiménez María-Josefa

Funder

Fondo de Investigaciones Sanitarias

Fundación Mutua Madrileña de Investigación Biomédica

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference37 articles.

1. HFE-associated hereditary hemochromatosis;Alexander;Genet Med,2009

2. Iron-overload-related disease in HFE hereditary hemochromatosis;Allen;N. Engl. J. Med.,2008

3. Lipid raft-dependent endocytosis: a new route for hepcidin-mediated regulation of ferroportin in macrophages;Auriac;Haematologica,2010

4. Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in Spain;Bach;Blood Cells Mol. Dis.,2006

5. A previously undescribed nonsense mutation of the HFE gene;Beutler;Clin. Genet.,2002

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