The CRISPR gene-editing technology is revolutionizing modern medicine, offering unprecedented possibilities for treating genetic disorders. By allowing precise modifications to DNA, CRISPR provides hope for curing previously untreatable diseases. Scientists and researchers continue to explore its applications, making it a promising tool for future medical breakthroughs. CRISPR stands for “Clustered Regularly Interspaced Short Palindromic Repeats,” a natural defense mechanism found in bacteria. The system uses the Cas9 protein to cut DNA at specific locations, enabling targeted genetic modifications.
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