.Kaufmann, P., Pariser, A. R. & Austin, C. From medical exploration to treatments for rare diseasesu00e2 $" the sight coming from the National Facility for Advancing Translational Sciencesu00e2 $" Office of Rare Diseases Research Study. Orphanet J. Rare Dis. Thirteen, 196 (2018 ). Articleu00c2.PubMedu00c2.Google.com Scholaru00c2.Crooke, S. T. A phone call to upper arms versus ultra-rare ailments. Nat. Biotechnol. 39, 671u00e2 $ "677 (2021 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Vockley, J. et al. The developing function of clinical geneticists in the age of genetics therapy: a necessity to prepare. Genet. Med. 25, 100022 (2023 ). Articleu00c2.CASu00c2.PubMedu00c2.Google Scholaru00c2.Kim, J. et al. Patient-customized oligonucleotide treatment for an unusual genetic condition. N. Engl. J. Med. 381, 1644u00e2 $ "1652 (2019 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Kim, J. et cetera. A structure for individualized splice-switching oligonucleotide treatment. Character 619, 828u00e2 $ "836 (2023 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Lima, W. F. et al. Individual RNase H1 differentiates between refined variations in the construct of the heteroduplex substrate. Mol. Pharmacol. 71, 83u00e2 $ "91 (2007 ). Articleu00c2.CASu00c2.PubMedu00c2.Google Scholaru00c2.Crooke, S. T., Baker, B. F., Crooke, R. M. & Liang, X.-H. Antisense modern technology: an overview as well as program. Nat. Rev. Drug Discov. Twenty, 427u00e2 $ "453 (2021 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Lee, J.-R. et al. Afresh mutations in the motor domain of KIF1A cause intellectual disability, abnormal paraparesis, axonal neuropathy, as well as cerebellar atrophy. Hum. Mutat. 36, 69u00e2 $ "78 (2015 ). Articleu00c2.CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Boyle, L. et al. Genotype as well as defects in microtubule-based motility connect along with medical extent in KIF1A-associated nerve condition. HGG Adv. 2, 100026 (2021 ). CASu00c2.PubMedu00c2.Google.com Scholaru00c2.Kondo, M., Takei, Y. & Hirokawa, N. Motor healthy protein KIF1A is vital for hippocampal synaptogenesis as well as knowing augmentation in an enriched environment. Nerve cell 73, 743u00e2 $ "757 (2012 ). Articleu00c2.CASu00c2.PubMedu00c2.Google Scholaru00c2.Guo, Y. et cetera. An unusual KIF1A missense mutation improves synaptic functionality and improves confiscation activity. Face. Genet. 11, 61 (2020 ). Articleu00c2.CASu00c2.PubMedu00c2.PubMed Centralu00c2.Google Scholaru00c2.Kaur, S. et al. Development of the phenotypic spectrum of de novo missense versions in kinesin family member 1A (KIF1A). Hum. Mutat. 41, 1761u00e2 $ "1774 (2020 ). Articleu00c2.CASu00c2.PubMedu00c2.PubMed Centralu00c2.Google Scholaru00c2.Canivez, G. L. & McGill, R. J. Aspect construct of the Differential Potential Scales-Second Version: exploratory and also ordered element analyses with the primary subtests. Psychol. Assess. 28, 1475u00e2 $ "1488 (2016 ). Articleu00c2.PubMedu00c2.Google.com Scholaru00c2.Epstein, A. et cetera. Web content validation of the quality of life inventoryu00e2 $" special needs. Childcare Health And Wellness Dev. 45, 654u00e2 $ "659 (2019 ). Articleu00c2.PubMedu00c2.Google.com Scholaru00c2.Lek, M. et cetera. Review of protein-coding hereditary variety in 60,706 humans. Attribute 536, 285u00e2 $ "291 (2016 ). Articleu00c2.CASu00c2.PubMedu00c2.Google Scholaru00c2.IND Submissions for Individualized Antisense Oligonucleotide Drug Products for Gravely Exhausting or Dangerous Health Conditions: Clinical Recommendations (US Fda, 2022) https://www.fda.gov/regulatory-information/search-fda-guidance-documents/ind-submissions-individualized-antisense-oligonucleotide-drug-products-severely-debilitating-or-lifeIND Entries for Personalized Antisense Oligonucleotide Medicine Products: Administrative as well as Step-by-step Suggestions Direction 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 Medicine Application Entries for Individual Antisense Oligonucleotide Medicine Products for Significantly Exhausting or even Lethal Diseases: Chemistry, Production, and also Controls Recommendations, Direction for Sponsor-Investigators (United States Food and Drug Administration, 2022) https://www.fda.gov/regulatory-information/search-fda-guidance-documents/investigational-new-drug-application-submissions-individualized-antisense-oligonucleotide-drugNonclinical Screening of Individualized Antisense Oligonucleotide Medicine Products for Seriously Devastating or Serious Ailments Support 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.