CTNNB1 Gene Therapy Foundation
We have started the CTNNB1 Gene Therapy Foundation in Texas to support gene therapy trials for children with CTNNB1 syndrome. The CTNNB1 Foundation is leading the charge in finding a cure. The gene therapy trial is set to begin in 2025 in Europe. Our mission is to raise awareness and support for CTNNB1 gene therapy, advocating for transformative research and treatments that offer hope to individuals and families affected by CTNNB1-related disorders. Through education, community engagement, and fundraising, we aim to drive forward gene therapy trials initiated by the CTNNB1 Foundation in Europe, accelerating the path to life-changing therapies and improving the quality of life for those in need.
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358. CTNNB1 Gene Therapy Foundation
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