The metabolomic plasma profile of patients with Duchenne muscular dystrophy: providing new evidence for its pathogenesis
Abstract Background Duchenne muscular dystrophy (DMD) is a fatal genetic muscle-wasting disease that affects 1 in 5000 male births with no current cure. Despite great progress has been made in the research of DMD, its underlying pathological mechanism based on the metabolomics is still worthy of fur...
| Published in: | Orphanet Journal of Rare Diseases |
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| Main Authors: | , , , , |
| Format: | Article |
| Language: | English |
| Published: |
BMC
2023-09-01
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| Subjects: | |
| Online Access: | https://doi.org/10.1186/s13023-023-02885-1 |