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Base editing: advances and therapeutic opportunities.

Nature reviews. Drug discovery · 2020 · Vol. 19 (12) · pp. 839-859

Abstract

Base editing - the introduction of single-nucleotide variants (SNVs) into DNA or RNA in living cells - is one of the most recent advances in the field of genome editing. As around half of known pathogenic genetic variants are due to SNVs, base editing holds great potential for the treatment of numerous genetic diseases, through either temporary RNA or permanent DNA base alterations. Recent advances in the specificity, efficiency, precision and delivery of DNA and RNA base editors are revealing exciting therapeutic opportunities for these technologies. We expect the correction of single point mutations will be a major focus of future precision medicine.

Publication Types

["Journal Article", "Review"]

Keywords

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MeSH Terms

["CRISPR-Cas Systems", "Disease", "Gene Editing", "Hearing Loss", "Humans", "Liver Diseases", "Muscular Dystrophy, Duchenne", "Neoplasms", "Polymorphism, Single Nucleotide"]

Funding

R01 NS103172 NINDS NIH HHS (United States)
R01 EY029166 NEI NIH HHS (United States)
R21 GM135736 NIGMS NIH HHS (United States)
T32 GM008326 NIGMS NIH HHS (United States)