ATP Binding Cassette Subfamily D Member 3 Gene Mutation
1 clinical trials · Condition
◉ Watch ATP Binding Cassette Subfamily D Member 3 Gene Mutation
| Record | Firm | Date |
|---|---|---|
| Longitudinal Natural History Study of Patients With Peroxisome Biogenesis Disorders (PBD) (NCT01668186) | McGill University Health Centre/Research Institute of the McGill University Health Centre | 2012-01-01 |
Track ATP Binding Cassette Subfamily D Member 3 Gene Mutation automatically
Every clearance here is in the API, with alerts when new ones post.