Associated Papers
Correction of human nonsense mutation via adenine base editing for Duchenne muscular dystrophy treatment in mouse.
Jin M et al.
Molecular Therapy. Nucleic Acids, 2024
38571746 (PubMed )
Supplement: mmc1.pdf
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
Comparison of The Carrier Frequency of Pathogenic Variants of DMD Gene in an Indian Cohort.
Nagabushana D et al.
Journal of Neuromuscular Diseases, 2021
Clinical and mutational characteristics of Duchenne muscular dystrophy patients based on a comprehensive database in South China.
Wang DN et al.
Neuromuscular Disorders : Nmd, 2017
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