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The deficiency is typically inherited in an autosomal recessive pattern, meaning both copies of the gene in each cell have mutations
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and certain disease states (see Primary systemic carnitine deficiency) (12)
This reaction is catalyzed by glutathione peroxidase (GPx), producing oxidized GSSG, which is subsequently recycled back to GSH by glutathione reductase
When food enters the gut, nutrients signal these cells to release GLP-1
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