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- W2023185610 abstract "We describe a 21-year-old man who developed copper deficiency manifested as a demyelinating neuropathy, chronic intestinal pseudo-obstruction, osteoporosis, testicular failure, retinal degeneration, and cardiomyopathy with a tortuous aorta. His serum copper was low and did not increase despite administration of large doses of intravenous copper sulfate. The ceruloplasmin level as measured by an antibody technique was normal, yet ceruloplasmin (Cp) oxidase activity was very low. The Cp amino acid sequence was normal. This suggests that the copper deficiency was caused by a defect in hepatic processing of copper for incorporation into Cp." @default.
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- W2023185610 date "1994-12-01" @default.
- W2023185610 modified "2023-10-16" @default.
- W2023185610 title "Copper deficiency secondary to a copper transport defect: A new copper metabolic disturbance" @default.
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- W2023185610 doi "https://doi.org/10.1016/0026-0495(94)90002-7" @default.
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