Mutation-independent proteomic signatures of pathological progression in murine models of Duchenne muscular dystrophy
The absence of the dystrophin protein in Duchenne muscular dystrophy (DMD) results in myofiber fragility and a plethora of downstream secondary pathologies. While a variety of experimental therapies are in development, achieving effective treatments for DMD remains exceptionally challenging, not lea...
| Prif Awduron: | , , , , , , , , , , , , , |
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| Fformat: | Journal article |
| Iaith: | English |
| Cyhoeddwyd: |
American Society for Biochemistry and Molecular Biology
2020
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