Larissa Nitschke

Feb 11, 2025 | jci.org | Yi Zhang |Larissa Nitschke |Sara Johnson |Rong-Chi Hu

ResearchGeneticsTherapeuticsOpen Access | 10.1172/JCI186416 J Clin Invest. https://doi.org/10.1172/JCI186416. Copyright © 2025, Hu et al. This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. View PDF AbstractMyotonic Dystrophy Type 1 (DM1) is an autosomal dominant disease caused by a CTG repeat expansion in the DMPK gene.