Article
Cognitive Impairment In Stable Wilson Disease Across Phenotype.
2021-05-17
Abstract excerpt
<title>Abstract</title> <p><bold>Background:</bold> In Wilson disease (WD), mutations in the gene encoding the ATP7B copper transport protein causes accumulation of copper especially in liver and brain. WD typically presents with hepatic and/or neuropsychiatric symptoms. Impaired cognition is a well-described feature in patients neurological WD, while the reports on cognition in hepatic WD patients are fewer and...
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Identifiers and source
- Literature Corpus work
- e6d9a7ed-950b-56d7-9939-bc68e02414ad
- DOI
- 10.21203/rs.3.rs-492155/v1