Nexa News

Researchers at the Global Institute of Genetics have developed PrecisionCRISPR, a groundbreaking gene editing technology that promises to revolutionize the treatment of inherited diseases. Clinical trials are set to begin later this year, offering new hope for conditions like Cystic Fibrosis and Huntington's Disease.

Researchers at the Institute of Genetic Medicine have developed a novel gene therapy approach that shows promise in treating rare genetic disorders. This breakthrough could revolutionize the field of gene therapy and offer hope to patients with currently untreatable conditions.