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Publikováno v:
Journal of Evidence Based Medicine and Healthcare, Vol 3, Iss 89, Pp 4853-4855 (2016)
BACKGROUND Thalassemia major patients are dependent on frequent blood transfusion and consequently develop iron overload. HFE gene mutations (C282Y, H63D and S65C) in hereditary haemochromatosis has been shown to be associated with iron overload. The