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In contrast, in heterozygous thalassemia, there is an inherited slow red-cell metabolism of riboflavin to FMN and FAD and a high stimulation of the erythrocyte glutathionine reductase by extraneous FAD (Anderson et al., 1993)

This simple adjustment ensures that you aren't just taking supplements, but actually absorbing and utilizing them to their full potential

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SKBK, TM, FZ summarized the table and made the figures

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