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Abstract
CRISPR technology has evolved significantly, focusing on precision in genome editing.
- Early CRISPR-Cas9 systems were efficient in targeting specific DNA sequences but raised concerns about unintended edits.
- The review discusses the transition of CRISPR from a prokaryotic discovery to its role in precision medicine.
- Current applications of CRISPR include targeted therapies for genetic disorders.
- Technical challenges such as off-target effects and delivery inefficiencies remain significant.
- Ethical considerations regarding accessibility and long-term impacts are also highlighted.
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