Wilson's Disease Gene Therapy and Molecular Research Trends for 2026
Restoring Liver Function through Single Dose Viral Vectors By 2026, gene therapy is expected to transition from an experimental concept to a viable clinical option for many living with Wilson's Disease. The goal of this research is to use modified viral vectors to deliver a functional copy of the ATP7B gene directly to the liver cells. In 2026 and 2026, early-stage human trials demonstrated...
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