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Analytical testing confirms above 99.8 percent purity assay content of 10.57 mg RT identification 0.997 spectrum 998 endotoxin below 0.001 EU per mg and no detectable heavy metals or microbial contamination

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Consistent with a link between low selenium and the effects of the GPx1 polymorphisms, in regions endemic for Keshan disease, there was a significant difference in the distribution of alleles in cases and controls, with a greater risk for individuals with the Pro/Leu or Leu/Leu genotypes of developing Keshan disease [36]

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