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Clinical trial

Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN

NCT05499091 is registered in ClinicalTrials.gov with University Hospital, Angers as lead sponsor.

NCT NCT05499091
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Registry record

As filed in ClinicalTrials.gov.

Title
Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN
Lead sponsor
University Hospital, Angers
Phase
Not applicable
Overall status
Recruiting
Start date
October 10, 2022
Completion date
October 10, 2045
Enrollment
1,200 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

genetic disease, rare diseases