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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

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The most extensively studied are those affecting the pathogens interaction with host cells, both epithelial and immune system cells, with a consequence of inducing gastric cancer development

DHAR, dehydroascorbate reductase

404,405,406 These cells not only respond to signals from leptin and insulin but also adapt to alterations in brain metabolism to accommodate behavioral changes by controlling glucose transport