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- W2063561285 abstract "The diagnosis of Wilson's disease is usually based on such biochemical findings as low serum caeruloplasmin, excess urinary copper excretion, and/or a high hepatic copper content. However, difficulties may arise in very young patients with this disease, since some of these biological features may not be present. We have diagnosed the disease in an 8-month-old baby on the basis of gene analysis." @default.
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- W2063561285 date "1997-06-01" @default.
- W2063561285 modified "2023-10-14" @default.
- W2063561285 title "Molecular diagnosis of Wilson's disease" @default.
- W2063561285 cites W2031579849 @default.
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- W2063561285 doi "https://doi.org/10.1016/s0140-6736(05)61691-1" @default.
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