The BALB/c.mdx62 mouse exhibits a dystrophic muscle pathology and is a model of Duchenne muscular dystrophy
oleh: Kristy Swiderski, Audrey S. Chan, Marco J. Herold, Andrew J. Kueh, Jin D. Chung, Justin P. Hardee, Jennifer Trieu, Annabel Chee, Timur Naim, Paul Gregorevic, Gordon S. Lynch
| Format: | Article |
|---|---|
| Diterbitkan: | The Company of Biologists 2024-04-01 |
Deskripsi
Subjek
muscular dystrophy; skeletal muscle; bone; pathophysiology; preclinical; genetic modifier