Key result
Human genetic studies and animal models have revealed distinct molecular and cellular mechanisms linking genetic mutations to diverse muscle wasting phenotypes in muscular dystrophy.
Design
Review
Authors
Loading...
Encourages genotype-specific dystrophy research; leaves open clinical translation of targeted therapies.
This review summarizes the molecular and cellular mechanisms linking genetic mutations to muscle degeneration in muscular dystrophies.
Rahimov et al. (2013) conducted a review in Muscular dystrophy. Human genetic studies and animal models have revealed distinct molecular and cellular mechanisms linking genetic mutations to diverse muscle wasting phenotypes in muscular dystrophy.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: