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RE: LeoThread 2025-04-06 04:45

in LeoFinance6 months ago

Part 4/9:

At the heart of this revolutionary approach is CRISPR-Cas9—an inexpensive and efficient method for genetic modification. Scientists discovered a technique whereby they can cut specific segments of DNA, opening the door to replacing faulty genes with healthy alternatives. For instance, a predisposition to hemophilia could theoretically be addressed by removing the faulty gene and replacing it with the normal gene.