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Effect of the Hemochromatosis Mutations on Iron Overload among the Indian β Thalassemia Carriers
BACKGROUND: Hereditary hemochromatosis is a disorder of iron metabolism characterized by increased iron absorption.HFE gene mutations C282Y and H63D are responsible for the majority of hereditary hemochromatosis cases. METHODS: We tried to look at the effect of HFE mutations on the iron status. A to...
Gorde:
Argitaratua izan da: | J Clin Lab Anal |
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Egile Nagusiak: | , , , , , |
Formatua: | Artigo |
Hizkuntza: | Inglês |
Argitaratua: |
John Wiley and Sons Inc.
2016
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Gaiak: | |
Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6816897/ https://ncbi.nlm.nih.gov/pubmed/27561698 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.22054 |
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