Quality of life and depression in Wilson’s disease: a large prospective cross-sectional study
Abstract Background Wilson's disease (WD) is an autosomal recessive genetic disorder due to a mutation of the ATP7B gene, resulting in impaired hepatic copper excretion and accumulation in various tissues. Lifelong decoppering treatments are the keystone of the treatment. These treatments can p...
Main Authors: | Kevin Chevalier, Djamila Rahli, Louise de Veyrac, Jessica Guillaume, Michaël Alexandre Obadia, Aurélia Poujois |
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Format: | Article |
Language: | English |
Published: |
BMC
2023-06-01
|
Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13023-023-02777-4 |
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