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...
| Những tác giả chính: | , , , , , , , , , , , , , |
|---|---|
| Định dạng: | Journal article |
| Ngôn ngữ: | English |
| Được phát hành: |
American Society for Biochemistry and Molecular Biology
2020
|