HIBM
1 clinical trials · Condition
| Record | Firm | Date |
|---|---|---|
| Clinical, Biological and NMR Outcome Measures Study for Hereditary Inclusion Body Myopathy Due to Mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine Kinase Gene (GNE) (NCT02196909) | Institut de Myologie, France | 2014-07-01 |
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