CRISPR Base Editing Repairs Hard-to-Treat Cystic Fibrosis Mutation in Cell Models
By applying base editing, scientists repaired a cystic fibrosis mutation that is unresponsive to current drugs in cell and organoid models, pointing to a possible treatment for some patients. The post CRISPR Base Editing Repairs Hard-to-Treat Cystic Fibrosis Mutation in Cell Models appeared first on GEN - Genetic Engineering and Biotechnology News.
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