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Wilson's disease is a genetic disorder, resulting from an anomaly present on the ATP7B gene located on chromosome 13, causing a progressive accumulation of copper in various organs such as the liver, ...
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Lead Sponsor
Centre Hospitalier Universitaire de Saint Etienne
NCT07301216 · Wilson Disease
NCT06650319 · Wilson Disease
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NCT05444127 · Wilson Disease
NCT05783687 · Wilson Disease
Hospices Civils de Lyon
Bron
Hôpital Nord CHU de Saint-Étienne
Saint-Etienne
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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