Associated Papers
Replacing the SpCas9 HNH domain by deaminases generates compact base editors with an alternative targeting scope.
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Molecular Therapy. Nucleic Acids, 2021
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Supplement: mmc3.xlsx › Tabelle1
Efficient precise in vivo base editing in adult dystrophic mice.
Xu L et al.
Nature Communications, 2021
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Supplement: 41467_2021_23996_MOESM1_ESM.pdf
Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan.
Okubo M et al.
Orphanet Journal of Rare Diseases, 2017
28859693 (PubMed )
Supplement: 13023_2017_703_MOESM1_ESM.pdf
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