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Between 2015 and 2023, the FDA issued 14 warning letters to companies selling glutathione products, nearly all for one of three violations: making unapproved disease treatment claims, selling adulterated products (contamination with heavy metals or incorrect active ingredient levels), or marketing injectable glutathione without a prescription
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Further delineation of pontocerebellar hypoplasia type 6 due to mutations in the gene encoding mitochondrial arginyl-tRNA synthetase, RARS2
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