Field dossier · from the corpus
Duchenne muscular dystrophy
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Most cited work
Circ-ZNF609 Is a Circular RNA that Can Be Translated and Functions in Myogenesis
Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy
Long-term evaluation of AAV-CRISPR genome editing for Duchenne muscular dystrophy
Muscle-specific CRISPR/Cas9 dystrophin gene editing ameliorates pathophysiology in a mouse model for Duchenne muscular dystrophy
A Single CRISPR-Cas9 Deletion Strategy that Targets the Majority of DMD Patients Restores Dystrophin Function in hiPSC-Derived Muscle Cells
Assessment of the Gene Therapy Immune Response in the Canine Muscular Dystrophy Model