Viewing StudyNCT00422721



Ignite Creation Date: 2024-05-05 @ 5:17 PM
Last Modification Date: 2024-10-26 @ 9:30 AM
Study NCT ID: NCT00422721
Status: COMPLETED
Last Update Posted: 2011-11-24
First Post: 2007-01-12

Brief Title: Genetic Study of Patients Suffering From Congenital Amaurosis of Leber or From an Early Severe Retinal Dystrophy
Sponsor: Nantes University Hospital
Organization: Nantes University Hospital

Conditions & Keywords Data

Conditions:
Name
Retinal Diseases
Amaurosis
Keywords:
Name View
amaurosis of leber View
early severe retinal dystrophy View