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However, we are on the cusp of trying to cure Wilson disease by genetically modifying the liver so it can produce a protein that is missing in patients with Wilson disease

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Shown is the phagocytosis by THP-1 cells (panel A) of ring-infected and non-infected GR-deficient RBCs from the index patient, brother (individual 2) and sister (individual 3) of the index patient, and from normal GR-sufficient controls

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