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Metabolic Features of Neurofibromatosis Type 1 Associated Tumors IntechOpen neurofibromotosis glutathione 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 Cell autonomous requirement of Neurofibromin (Nf1) for postnatal muscle hypertrophic growth and metabolic homeostasis bioRxiv Functional Assays Combined with PremRNASplicing Analysis Improve Variant Classification and Diagnostics for Individuals with Neurofibromatosis Type 1 and Legius Syndrome Douben 2023 Human Mutation Wiley Online Library Loss of neurofibromin induces inflammatory macrophage phenotypic switch and retinal neovascularization via GLUT1 activation ScienceDirect
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