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Three Novel Enhanced Delivery Oligonucleotide (EDO) Candidates for Duchenne Muscular Dystrophy Mediated High Levels of Exon 53, 45, and 44 Skipping
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PGN-EDODM1 Nonclinical Data Demonstrate Mechanistic and Meaningful Activity for Potential Treatment of Myotonic Dystrophy Type 1
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PGN-EDODM1 Nonclinical Data Demonstrated Mechanistic and Meaningful Activity for the Potential Treatment of Myotonic Dystrophy Type 1 (DM1)