Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN
Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN
Recruiting · NCT05499091 · Registry updated 2026-06-29Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, hereditary disease | Recruiting | Not applicable | 2026-06-29 | NCT05499091 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| University Hospital, Angers | 123 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Centre Hospitalo-Universitaire d'Angers | Angers | France | 2 |