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Antiviral and immunomodu-latory properties of new pro-glutathione (GSH) molecules

Wilson disease Wilson disease Wilson disease (hepatolenticular degeneration) is an autosomal recessive disorder caused by various mutations in the ATP7B gene, which regulates copper transport within hepatocytes

Zeng, Z

Exp Mol Med 54(9):14011411

Additionally, we provide guidelines for data interpretation, quantification, and statistical analysis to ensure robust and reliable results

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