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In addition, as the number of PSCs and pancreatic fibrosis increased, -cell function was significantly impaired

Neuropsychiatric manifestations differentiate 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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Over-Expression of Lncrna Tmem161b-As1 Promotes the Malignant Biological Behavior of Glioma Cells and the Resistance to Temozolomide Via Up-Regulating the Expression of Multiple Ferroptosis-Related Genes by Sponging Hsa-Mir-27a-3p