MYT1L Syndrome: a Rare Paediatric Genetic Syndrome Responsible for a Neurodevelopmental Disorder
Clinical trial NCT07008612 · RECRUITING
Trial details
- NCT number
- NCT07008612
- Sponsor
- University Hospital, Rouen
- Status
- RECRUITING
- Phase
- Not Applicable
- Study type
- INTERVENTIONAL
- Start date
- 2025-02-04
- Primary completion
- 2027-05-01
- Enrollment
- 50
Track trials programmatically
Sponsors, conditions and status changes through the Atlas API.