Long-term maintenance of dystrophin expression and resistance to injury of skeletal muscle in gene edited DMD mice
Duchenne muscular dystrophy (DMD) is a lethal muscle disease caused by mutations in the dystrophin gene. CRISPR/Cas9 genome editing has been used to correct DMD mutations in animal models at young ages. However, the longevity and durability of CRISPR/Cas9 editing remained to be determined. To addres...
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Elsevier,
2022-06-01T00:00:00Z.
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