[2S08m] FAONS Symposium
Unlocking Hope : Viral vector-mediated gene therapy for neurological disorders-A promising frontier in therapeutic advancements and future prospects

[2S08m-04] Gene replacement therapy in a schwannomamouse
model of neurofibromatosis type 2

*Pike See Cheah^1,2, Shilpa Prabhakar², Xandra Breakefield² (1. Universiti Putra Malaysia, 2. Massachusetts General Hospital, Harvard Medical School, Boston, USA)

Keywords:gene therapy, AAV, Neurofibromatosis, mouse