Associated Papers
Precise correction of a spectrum of β-thalassemia mutations in coding and non-coding regions by base editors.
Prasad K et al.
Molecular Therapy. Nucleic Acids, 2024
38817682 (PubMed )
Supplement: mmc3.pdf
Correction of β-thalassemia mutant by base editor in human embryos.
Liang P et al.
Protein & Cell, 2017
The mechanism by which TATA-box polymorphisms associated with human hereditary diseases influence interactions with the TATA-binding protein.
Drachkova I et al.
Human Mutation, 2014
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