NCT00004815
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, DNA Repair-Deficiency Disorders, Disease Attributes, +8 more
- Locations
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Not specified
Clinical trial condition
Werner's Syndrome
Explore clinical trials studying Werner's Syndrome. Study availability and eligibility vary by location and protocol.
1 public trial
0 recruiting studies