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References: Barclay, R

Glutathione synthase (GSS) deficiency is an inherited autosomal recessive disease caused by genetic mutations in the GSS gene that codes for the GSS enzyme

Sex differences in markers of oxidation and inflammation

Environmental Science & Technology, 49 (19), 1134811355

The Phase 1 trial in 80 healthy volunteers demonstrated safety and tolerability across four dose levels with no serious adverse events

Through the N-ethyl-N-nitrosourea (ENU) mutagenesis protocol in mice, it was reported that Slc4a10, encoding solute carrier family 4, sodium bicarbonate transporter, member 10, is a novel late-onset hearing loss gene, critical to inner ear homeostasis [37]