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Firoozrai, H

In the Turkish population, the GSTM1 -null variant was expressed in around half of the patients with lung cancer compared to a slightly higher prevalence of 52.6% in the control group [17]

Free Radic Biol Med 102:203216

Mice lacking the intestinal and renal neutral amino acid transporter SLC6A19 demonstrate the relationship between dietary protein intake and amino acid malabsorption

Most GHI cases have autosomal recessive inheritance and in the vast majority a molecular defect has been identified involving homozygous or compound heterozygous mutations (Lupu et al., 2001)

It can remove multiple oxidants and is rapidly recycled back to its active form by co-factors in your body like glutathione (GSH)