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The G6PD deficiency still prevails as the most common of all the inherited enzymatic defects 22,23 and it is clinically significant not only in the hematological field but also in the human biology 24 and it is characterized by a large biochemical and genetic heterogeneity
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(Removed: "Treatment of Non-Alcoholic Fatty Liver Disease") alamon , Kramar B, Marolt TP, Poljak B, Milisav I
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