Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy (Q37651944)

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scientific article published on 14 February 2017
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Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
scientific article published on 14 February 2017

    Statements

    Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy (English)
    Niclas E Bengtsson
    John K Hall
    Guy L Odom
    Michael P Phelps
    Colin R Andrus
    R David Hawkins
    Stephen D Hauschka
    Joel R Chamberlain
    Jeffrey S Chamberlain
    14 February 2017
    14454

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