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In early stages, 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

Adducts of dienochlor miticide with glutathione, glutathione S-transferases, and [PMID: 7981413] Laboratory literature summary: Adducts of dienochlor miticide with glutathione, glutathione S-transferases, and hemoglobins

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