NCT00373165
- Conditions
- Amino Acid Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cytomegalovirus Infection, +12 more
- Locations
-
Not specified
Clinical trial condition
Explore clinical trials studying Multiple Acyl Coenzyme A Dehydrogenase Deficiency. Study availability and eligibility vary by location and protocol.
NCT00373165
Not specified
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