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Breakthrough in Gene Editing: New Hope for Rare Diseases in 2025
6/9/2025Medical Research

Breakthrough in Gene Editing: New Hope for Rare Diseases in 2025

Researchers at the Global Health Institute have made significant progress in gene editing technology using CRISPR-Cas9, offering new hope for patients with rare genetic diseases. This breakthrough paves the way for personalized treatments and could revolutionize healthcare.
Gene EditingCRISPR-Cas9rare diseasesPersonalized Medicinegenetic disordersmedical researchhealthcare innovation
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