Page 39 - Read Online
P. 39
Okaz et al. Rare Dis Orphan Drugs J. 2025;4:24 https://dx.doi.org/10.20517/rdodj.2025.15 Page 11 of 11
depletion. Nat Commun. 2021;12:4358. DOI PubMed PMC
42. Osum SH, Oribamise EI, Corbière SMAS, et al. Combining nonsense mutation suppression therapy with nonsense-mediated decay
inhibition in neurofibromatosis type 1. Mol Ther Nucleic Acids. 2023;33:227-39. DOI PubMed PMC
43. Exploring Nonsense Suppression as a Treatment for NF1. Synapse: syn2164183. DOI
44. Takeda S, Clemens PR, Hoffman EP. Exon-Skipping in Duchenne Muscular Dystrophy. J Neuromuscul Dis. 2021;8:S343-58. DOI
PubMed PMC
45. McCauley ME, Bennett CF. Antisense drugs for rare and ultra-rare genetic neurological diseases. Neuron. 2023;111:2465-8. DOI
PubMed
46. Leier A, Moore M, Liu H, et al. Targeted exon skipping of NF1 exon 17 as a therapeutic for neurofibromatosis type I. Mol Ther
Nucleic Acids. 2022;28:261-78. DOI PubMed PMC
47. Church C. Targeted Exon Skipping of NF1 Exon 52 as a Mutation-Specific Therapeutic for Neurofibromatosis Type 1. 2024 Global
NF Conference; 2024 Jun 20-25; Brussels, Belgium. Available from https://www.ctf.org/wp-content/uploads/2024/06/24_
NFConferenceAbstractBook_web.pdf [accessed 26 August 2025].
48. Lehtonen A, Howie E, Trump D, Huson SM. Behaviour in children with neurofibromatosis type 1: cognition, executive function,
attention, emotion, and social competence. Dev Med Child Neurol. 2013;55:111-25. DOI PubMed
49. Botero V, Tomchik SM. Unraveling neuronal and metabolic alterations in neurofibromatosis type 1. J Neurodev Disord. 2024;16:49.
DOI PubMed PMC
50. Kim TY, Siesser PF, Rossman KL, et al. Substrate trapping proteomics reveals targets of the βTrCP2/FBXW11 ubiquitin ligase. Mol
Cell Biol. 2015;35:167-81. DOI
51. Kohn DB, Chen YY, Spencer MJ. Successes and challenges in clinical gene therapy. Gene Ther. 2023;30:738-46. DOI PubMed
PMC
52. Gao J, Gunasekar S, Xia ZJ, et al. Gene therapy for CNS disorders: modalities, delivery and translational challenges. Nat Rev
Neurosci. 2024;25:553-72. DOI

