Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome-Reference-Cited by-同舟云学术

Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome

Published:2001-11 Issue:2 Volume:115 Page:334-340
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

Girelli Domenico,Bozzini Claudia,Zecchina Gabriella,Tinazzi Elisa,Bosio Sandra,Piperno Alberto,Ramenghi Ugo,Peters Jutta,Levi Sonia,Camaschella Clara,Corrocher Roberto

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2001.03116.x/fullpdf

Reference33 articles.

1. Clinical severity and thermodynamic effects of iron-responsive element mutations in hereditary hyperferritinemia-cataract syndrome;Allerson;Journal of Biological Chemistry,1999

2. Hyperferritinemia in the absence of iron overload;Arnold;Gut,1997

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

4. Description of a new mutation in the l-ferritin iron-responsive element associated with hereditary hyperferritinemia-cataract syndrome in a Spanish family;Balas;Blood,1999

5. Coinheritance of alleles associated with hemochromatosis and hereditary hyperferritinemia-cataract syndrome;Barton;Blood,1998

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