In a recent breakthrough, scientists have discovered the promise of a new approach to treating genetic insufficiency. This approach, known as “gene addition,” involves the insertion of a healthy gene into a person’s cells to replace a defective gene. This technique has shown to be an effective treatment for diseases caused by a single gene defect, such as hemophilia, cystic fibrosis, and Duchenne muscular dystrophy. It has also been used to treat certain types of cancer. This pioneering research has the potential to revolutionize gene therapy and unlock new treatments that will improve the lives of those suffering from genetic diseases.

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source: Phys.org