Commentary: Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage

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[34] Highly efficient endogenous human gene correction using designed zinc-finger nucleases [J]. NATURE, 2005, 435 (7042) : 646 - 651

[35] Veltman JA, 2012, NAT REV GENET, V13, P565, DOI 10.1038/nrg3241

[36] Delivery technologies for genome editing [J]. NATURE REVIEWS DRUG DISCOVERY, 2017, 16 (06) : 387 - 399

[37] CRISPR/Cas9 for genome editing: progress, implications and challenges [J]. HUMAN MOLECULAR GENETICS, 2014, 23 : R40 - R46

[38] DNA editing in DNA/RNA hybrids by adenosine deaminases that act on RNA [J]. NUCLEIC ACIDS RESEARCH, 2017, 45 (06) : 3369 - 3377

[31] CRISPR-Cas systems for editing, regulating and targeting genomes [J]. NATURE BIOTECHNOLOGY, 2014, 32 (04) : 347 - 355

[32] A combinatorial approach to create artificial homing endonucleases cleaving chosen sequences [J]. NUCLEIC ACIDS RESEARCH, 2006, 34 (22)

[33] A genome-editing strategy to treat β-hemoglobinopathies that recapitulates a mutation associated with a benign genetic condition [J]. NATURE MEDICINE, 2016, 22 (09) : 987 - +

[34] Highly efficient endogenous human gene correction using designed zinc-finger nucleases [J]. NATURE, 2005, 435 (7042) : 646 - 651

[35] Veltman JA, 2012, NAT REV GENET, V13, P565, DOI 10.1038/nrg3241

[36] Delivery technologies for genome editing [J]. NATURE REVIEWS DRUG DISCOVERY, 2017, 16 (06) : 387 - 399

[37] CRISPR/Cas9 for genome editing: progress, implications and challenges [J]. HUMAN MOLECULAR GENETICS, 2014, 23 : R40 - R46

[38] DNA editing in DNA/RNA hybrids by adenosine deaminases that act on RNA [J]. NUCLEIC ACIDS RESEARCH, 2017, 45 (06) : 3369 - 3377