Modifying multiple genes and hoping to treat diseases with CRISPR-Cas12a
Reading Time: 4 minutes A Swiss team figured out how to modify multiple genes in one cell using the gene-editing CRISPR-system Cas12a. What do the findings mean for disease treatment strategies? In May, during our Amsterdam S.H.I.T. Show, we talked about the gene-editing CRISPR-Cas systems and how they enable you to cut DNA almost anywhere you want. The tools…