
Groundbreaking Genetic Therapy Saves Child with Rare Disorder
Scientists use CRISPR gene editing to successfully treat a child with a rare and deadly genetic disorder, marking a major milestone in personalized genetic medicine.
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Scientists use CRISPR gene editing to successfully treat a child with a rare and deadly genetic disorder, marking a major milestone in personalized genetic medicine.
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Discover how CRISPR-Cas9, invented by Jennifer Doudna and Emmanuelle Charpentier, is transforming genetic engineering with its precision and potential to cure genetic diseases.