تحرير الجينات مع كريسبر/cas9: إحداث ثورة في علاج بيتا ثالاسيميا
**كريسبر/CAS9: A Revolutionary Gene Editing Tool for Beta-Thalassemia**
CRISPR/Cas9 gene editing technology has emerged as a promising therapeutic approach for beta-thalassemia, a genetic blood disorder. By precisely targeting and modifying the responsible genes, CRISPR/Cas9 offers the potential to correct genetic defects and restore normal hemoglobin production, revolutionizing treatment options for this debilitating condition.