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New progress in NF2 gene therapy ✨ CTF research published promising early steps toward a personalized gene therapy approach for NF2-related schwannomatosis—starting with patient-derived cells and advancing into more advanced tumor-like models. This research is still early, but it represents meaningful momentum for families living with NF2-SWN. Read what this progress could mean for the future: 🔗 https://www.ctf.org/news/nf2-gene-therapy-ctf-research-advances-a-promising-personalized-approach/ #
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New progress in NF2 gene therapy ✨ CTF research published promis…
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Children’s Tumor Foundation (CTF) – Young Investigator Award – Doctoral/Postdoctoral Fellowships for Neurofibromatosis Research
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vanderbilt.edu
Jake is raising his voice. CTF is driving the science. Together, we can ensure NF2-related schwannomatosis patients have more options, more paths forward, and more time. Progress in NF2 is accelerating — but funding must keep pace. 👉 Donate today: go.ctf.org/donate #EndNF #NF2 #NF2SWN #EndNF2 | Children's Tumor Foundation
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Jake is raising his voice. CTF is driving the science. Together, we …
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FacebookChildren's Tumor Foundation
Driving treatments for people living with NF1, NF2-related schwannomatosis, and schwannomatosis is at the heart of this work. Your support helps move science forward and brings answers closer. Give at go.ctf.org/donate and your impact will be doubled. Thanks to Pat Spencer, a dedicated supporter for over 29 years, who is matching donations up to $50,000 in honor of her son and grandson, who live with NF. Offline gifts (checks, DAFs, wire and stock transfers) will be matched once received and ver
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