Clinical trial
Identification of the Molecular and/or Pathophysiological Bases of Rare Diseases of Genetic Origin (or Rare Forms of Frequent Diseases Suspected of Being of Genetic Origin).
NCT03287193 is registered in ClinicalTrials.gov with Centre Hospitalier Universitaire Dijon as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Identification of the Molecular and/or Pathophysiological Bases of Rare Diseases of Genetic Origin (or Rare Forms of Frequent Diseases Suspected of Being of Genetic Origin).
- Lead sponsor
- Centre Hospitalier Universitaire Dijon
- Phase
- Observational
- Overall status
- Recruiting
- Start date
- March 13, 2017
- Completion date
- December 31, 2027
- Enrollment
- 850 (estimated)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
rare diseases of genetic origin, rare forms of common diseases suspected of being genetic in origin