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JOURNAL ARTICLE
Imprecision Medicine: A One-Size-Fits-Many Approach for Muscle Dystrophy.
Cell Stem Cell 2016 April 8
There is still no curative treatment for Duchenne muscular dystrophy (DMD). In this issue of Cell Stem Cell, Young et al. (2016) demonstrate a genome editing approach applicable to 60% of DMD patients with CRISPR/Cas9 using one pair of guide RNAs.
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