Engineering Biology
 2020
DOI: 10.1049/enb.2020.0017
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Gene modification strategies using AO‐mediated exon skipping and CRISPR/Cas9 as potential therapies for Duchenne muscular dystrophy patients

Marthe Helene Solberg
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,
Maryam Shariatzadeh
2
,
S. Wilson
3
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