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A human bioavailability trial performed in Finland with men of moderately low selenium status showed significant differences among various forms of selenium tested (e.g., selenate, wheat, yeast), depending on the criterion of availability used (increase in platelet GPX activity, elevation of plasma or red blood cell selenium content, retention of selenium) (14)

Dysregulation of these intricate networks can subsequently trigger cell death and contribute to the onset and progression of diseases such as NDDs, autoimmune diseases, and cancer

doi: 10.1007/s10803-018-3568-z 163 ShiL.SmithS

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