NCT02056912
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Lipid Metabolism Disorders, +7 more
- Locations
-
- Service de Génétique Médicale Bordeaux, France
Clinical trial condition
Explore clinical trials studying Lipodystrophy. Study availability and eligibility vary by location and protocol.
NCT02056912
NCT01784289
NCT03059121
NCT04656054
NCT05930106
NCT06089759
NCT05402982
NCT05239351
NCT05239156