Background. Neurofibromatosis type 1 is a genetic disorder caused by loss-of-function mutations in a tumor suppressor gene (NF1) which codifies the protein neurofibromin. The frequent genetic alterations that modify neurofibromin function are deletions and insertions. https://www.roneverhart.com/Vox-AC30S1-Single-Channel-1x12-Combo-p21102/