Gene Therapy Revolution: A Focus at Rare Disease Congress

Explore the future of rare disease treatment through gene therapy breakthroughs at the 5th World Congress in Paris. Sessions cover advancements in CRISPR, viral vector technologies, and long-term efficacy studies for conditions like SMA, hemophilia, and rare retinal disorders. Discover how biotech firms and academic researchers are transforming patient care with curative gene therapies. Meet pioneers in genetic medicine, regulatory leaders, and funding experts shaping the next era of precision therapeutics. Don’t miss this opportunity to dive deep into gene therapy's rare disease potential.

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