Is H63D a ‘minor’ HFE polymorphism?-Reference-Cited by-同舟云学术

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Is H63D a ‘minor’ HFE polymorphism?

Published:2015-12 Issue:10 Volume:38 Page:588-589
ISSN:0210-5705
Container-title:Gastroenterología y Hepatología
language:en
Short-container-title:Gastroenterología y Hepatología

Author:

Pinto-Pais Teresa,Fernandes Sónia,Fernandes Carlos,Ribeiro Iolanda,Leite Sónia,Silva Ana Paula,Alberto Luís,Fraga José,Carvalho João

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference5 articles.

1. EASL clinical practice guidelines for HFE hemochromatosis;European Association for the Study of the Liver;J Hepatol,2010

2. Hemochromatosis and iron-overload screening in a racially diverse population;Adams;N Engl J Med,2005

3. H63D homozygotes with hyperferritinaemia: is this genotype the primary cause of iron overload;De Diego;Eur J Haematol,2006

4. Variable phenotypic presentation of iron overload in H63D homozygotes: are genetic modifiers the cause;Aguilar-Martinez;Gut,2001

5. Iron overload is rare in patients homozygous for the H63D mutation;Kelley;Can J Gastroenterol Hepatol,2014

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Proven: The causative role of homozygous H63D mutation in hereditary haemochromatosis;Gastroenterología y Hepatología;2016-08

2. Proven: The causative role of homozygous H63D mutation in hereditary haemochromatosis;Gastroenterología y Hepatología (English Edition);2016-08

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