Associated Papers
Efficient precise in vivo base editing in adult dystrophic mice.
Xu L et al.
Nature Communications, 2021
34140489 (PubMed )
Supplement: 41467_2021_23996_MOESM1_ESM.pdf
Derivation and Characterization of Immortalized Human Muscle Satellite Cell Clones from Muscular Dystrophy Patients and Healthy Individuals.
Massenet J et al.
Cells, 2020
Exon skipping induced by nonsense/frameshift mutations in DMD gene results in Becker muscular dystrophy.
Okubo M et al.
Human Genetics, 2020
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