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Most diagnostically unsolved rare disease have a genetic cause. These causes have not been found applying the current methodologies due to technical limitations (e.g. repeat expansions, changes in non...
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Lead Sponsor
Centre Hospitalier Universitaire Dijon
NCT07527624 · Rare Diseases
NCT06595940 · Undiagnosed Diseases, Rare Diseases
NCT07247279 · Rare Diseases, Generalized Myasthenia Gravis (gMG)
NCT07102966 · Rare Diseases
NCT06573723 · Rare Diseases, Amyloidosis, and more
CHU de Dijon
Dijon
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Data Source & Attribution
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.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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