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Neurofibromatosis Type 1 is a genetic disorder characterized by multiple cutaneous neurofibromas, caf au lait macules, and systemic involvement due to NF1 gene mutation. Disclaimer For educational purposes only. Not medical advice. Consult a Translating current basic research into future therapies for neurofibromatosis type 1 British Journal of Cancer Neurofibromatosis type 1 (NF 1) Lisch Nodules. EyeRounds.org: Online Ophthalmic Atlas Tumorigenesis in neurofibromatosis type 1: role of the microenvironment Oncogene
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