Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle
Limb-girdle muscular dystrophy type 2A (LGMD2A) is a form of muscular dystrophy caused by mutations in calpain 3 (CAPN3). Several studies have implicated Ca2+ dysregulation as an underlying event in several muscular dystrophies, including LGMD2A. In this study we used mouse and human myotube culture...
| Main Authors: | , , , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Cambridge University Press
2016
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4836212/ |