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- W2890638010 endingPage "248" @default.
- W2890638010 startingPage "237" @default.
- W2890638010 abstract "Abstract Wilson disease (WD, OMIM #277900) is an autosomal recessive copper accumulation disorder mainly affecting the liver and the brain. WD is potentially fatal but effective treatment is available. The pivotal point to achieve the best outcome relies on a timely and accurate diagnosis. Historically, diagnosis of WD was based on the Sternlieb’s criteria with at least two of the followings: typical neurological symptoms, presence of Kayser-Fleischer rings by slit lamp examination and a serum ceruloplasmin concentration" @default.
- W2890638010 created "2018-09-27" @default.
- W2890638010 creator A5087202559 @default.
- W2890638010 date "2019-01-01" @default.
- W2890638010 modified "2023-09-25" @default.
- W2890638010 title "Biochemical Diagnosis of Wilson Disease" @default.
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- W2890638010 doi "https://doi.org/10.1016/b978-0-12-810532-0.00021-5" @default.
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