Pathogenesis of Hyperferritinemia Cataract Syndrome-Reference-Cited by-同舟云学术

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Pathogenesis of Hyperferritinemia Cataract Syndrome

Published:2002-11 Issue:3 Volume:29 Page:532-535
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Roetto Antonella,Bosio Sandra,Gramaglia Enrico,Barilaro Maria Rosa,Zecchina Gabriella,Camaschella Clara

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference11 articles.

1. Characterization and expression of iron regulatory protein 2 (IRP2);Guo;J. Biol. Chem.,1995

2. Cloning of the cDNA encoding an RNA regulatory protein-The human iron responsive element binding protein;Roualt;Proc. Natl. Acad. Sci USA,1990

3. Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA;Cazzola;Blood,1997

4. A novel deletion of the L-ferritin iron responsive element responsible for severe hyperferritinemia-cataract syndrome;Cazzola;Br. J. Haematol.,2002

5. Hereditary hyperferritinemia cataract syndrome: a de novo mutation in the iron responsive element of the L-ferritin gene;Arosio;Haematologica,1999

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