Leber Congenital Amaurosis 2
2 clinical trials · Condition
◉ Watch Leber Congenital Amaurosis 2
| Record | Firm | Date |
|---|---|---|
| Natural History of Patients With Inherited Retinal Diseases Due to Mutations in RPE65 Gene (NCT04525261) | University of Campania Luigi Vanvitelli | 2020-05-01 |
| Early Check: Expanded Screening in Newborns (NCT03655223) | RTI International | 2018-10-15 |
Track Leber Congenital Amaurosis 2 automatically
Every clearance here is in the API, with alerts when new ones post.