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).
Clinical trial NCT03287193 · RECRUITING
Trial details
- NCT number
- NCT03287193
- Sponsor
- Centre Hospitalier Universitaire Dijon
- Status
- RECRUITING
- Study type
- OBSERVATIONAL
- Start date
- 2017-03-13
- Primary completion
- 2027-03-01
- Enrollment
- 850
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