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...

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Vydáno v:J Clin Lab Anal
Hlavní autoři: Nadkarni, Anita H., Singh, Aradhana A., Colaco, Stacy, Hariharan, Priya, Colah, Roshan B., Ghosh, Kanjaksha
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2016
Témata:
Brief Reports
On-line přístup: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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