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Using gene therapy for the first time managed to prevent the development of blindness

As reported in the journal Nature Communications, a group of biologists from the U.S. for the first time were able to cure complete blindness in mice. The assurances of the newspaper, it was possible thanks to the use of the editor of the genome of CRISPR/Cas9. With it removed the defective gene responsible for the development of blindness.

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Using gene therapy for the first time managed to prevent the development of blindness

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