CRISPR gene editing has revolutionized the landscape of genetic science, offering unprecedented possibilities for treating hereditary diseases.This cutting-edge technology enables precise alterations in DNA, raising hopes for cures, such as gene editing for sickle cell disease.
CRISPR gene editing has emerged as a revolutionary technology in the field of genetics, promising the potential to not only treat but also cure life-threatening diseases such as sickle cell disease.This innovative technique allows scientists to precisely edit DNA, igniting a passionate debate surrounding gene editing ethics and the implications of genetic modification on health equity.