.Kaufmann, P., Pariser, A. R. & Austin, C. From clinical discovery to procedures for unusual diseasesu00e2 $" the viewpoint from the National Center for Evolving Translational Sciencesu00e2 $" Office of Rare Diseases Investigation. Orphanet J. Rare Dis. Thirteen, 196 (2018 ). Articleu00c2.PubMedu00c2.Google Scholaru00c2.Crooke, S. T. A contact us to arms against ultra-rare diseases. Nat. Biotechnol. 39, 671u00e2 $ "677 (2021 ). Articleu00c2.CASu00c2.PubMedu00c2.Google Scholaru00c2.Vockley, J. et al. The growing duty of health care geneticists in the era of gene therapy: an urgency to ready. Genet. Medication. 25, 100022 (2023 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Kim, J. et al. Patient-customized oligonucleotide treatment for an uncommon genetic condition. N. Engl. J. Medication. 381, 1644u00e2 $ "1652 (2019 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Kim, J. et cetera. A structure for personalized splice-switching oligonucleotide therapy. Structure 619, 828u00e2 $ "836 (2023 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Lima, W. F. et al. Human RNase H1 differentiates in between subtle variants in the framework of the heteroduplex substrate. Mol. Pharmacol. 71, 83u00e2 $ "91 (2007 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Crooke, S. T., Baker, B. F., Crooke, R. M. & Liang, X.-H. Antisense modern technology: an introduction and also prospectus. Nat. Rev. Drug Discov. Twenty, 427u00e2 $ "453 (2021 ). Articleu00c2.CASu00c2.PubMedu00c2.Google Scholaru00c2.Lee, J.-R. et cetera. Afresh mutations in the motor domain of KIF1A cause intellectual impairment, spastic paraparesis, axonal neuropathy, as well as cerebellar degeneration. Hum. Mutat. 36, 69u00e2 $ "78 (2015 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Boyle, L. et al. Genotype and also defects in microtubule-based mobility associate with medical intensity in KIF1A-associated neurological problem. HGG Adv. 2, 100026 (2021 ). CASu00c2.PubMedu00c2.Google Scholaru00c2.Kondo, M., Takei, Y. & Hirokawa, N. Motor protein KIF1A is actually essential for hippocampal synaptogenesis as well as finding out improvement in an enriched atmosphere. Neuron 73, 743u00e2 $ "757 (2012 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Guo, Y. et al. A rare KIF1A missense mutation enhances synaptic feature and enhances seizure task. Face. Genet. 11, 61 (2020 ). Articleu00c2.CASu00c2.PubMedu00c2.PubMed Centralu00c2.Google Scholaru00c2.Kaur, S. et cetera. Expansion of the phenotypic spectrum of afresh missense variants in kinesin relative 1A (KIF1A). Hum. Mutat. 41, 1761u00e2 $ "1774 (2020 ). Articleu00c2.CASu00c2.PubMedu00c2.PubMed Centralu00c2.Google Scholaru00c2.Canivez, G. L. & McGill, R. J. Element design of the Differential Potential Scales-Second Edition: exploratory and hierarchical aspect evaluations along with the core subtests. Psychol. Assess. 28, 1475u00e2 $ "1488 (2016 ). Articleu00c2.PubMedu00c2.Google.com Scholaru00c2.Epstein, A. et cetera. Information recognition of the quality of life inventoryu00e2 $" impairment. Childcare Health And Wellness Dev. Forty five, 654u00e2 $ "659 (2019 ). Articleu00c2.PubMedu00c2.Google.com Scholaru00c2.Lek, M. et al. Review of protein-coding genetic variety in 60,706 humans. Attributes 536, 285u00e2 $ "291 (2016 ). Articleu00c2.CASu00c2.PubMedu00c2.Google Scholaru00c2.IND Submissions for Individualized Antisense Oligonucleotide Medication Products for Badly Devastating or Serious Health Conditions: Professional Referrals (United States Fda, 2022) https://www.fda.gov/regulatory-information/search-fda-guidance-documents/ind-submissions-individualized-antisense-oligonucleotide-drug-products-severely-debilitating-or-lifeIND Submittings for Individual Antisense Oligonucleotide Drug Products: Managerial and Procedural Referrals Support for Sponsor-Investigators (US Food and Drug Administration, 2021) https://www.fda.gov/regulatory-information/search-fda-guidance-documents/ind-submissions-individualized-antisense-oligonucleotide-drug-products-administrative-and-proceduralInvestigational New Drug Use Submittings for Individual Antisense Oligonucleotide Medication Products for Severely Debilitating or even Severe Diseases: Chemistry, Production, as well as Controls Recommendations, Guidance for Sponsor-Investigators (United States Fda, 2022) https://www.fda.gov/regulatory-information/search-fda-guidance-documents/investigational-new-drug-application-submissions-individualized-antisense-oligonucleotide-drugNonclinical Testing of Individualized Antisense Oligonucleotide Medication Products for Gravely Devastating or even Lethal Diseases Assistance for Sponsor-Investigators (United States Food and Drug Administration, 2021) https://www.fda.gov/regulatory-information/search-fda-guidance-documents/nonclinical-testing-individualized-antisense-oligonucleotide-drug-products-severely-debilitating-or.