Duchenne muscular dystrophy

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Reference no: EM133822048

Question

What is the potential application of CRISPR in treating Duchenne muscular dystrophy (DMD)? The dystrophin gene can be removed from all cells. Corrections can be made to the dystrophin gene to restore function. It introduces mutations to accelerate disease progression. It decreases the production of functional dystrophin protein.

Reference no: EM133822048

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