Perelli, R. M., Sitton, M. J., Bohning, J. D., Pickar-Oliver, A., McCullough, K. T., Moya-Mendez, M. E., … Landstrom, A. P. (2025). Deletion of Exon 51 in a Humanized Duchenne Muscular Dystrophy Mouse Model Abolishes Ventricular Arrhythmia Predisposition. Circ Genom Precis Med, 18(3), e004867. https://doi.org/10.1161/CIRCGEN.124.004867

Perelli, Robin M., Madeleine J. Sitton, Joel D. Bohning, Adrian Pickar-Oliver, K Tyler McCullough, Mary E. Moya-Mendez, Scott Zheng, et al. “Deletion of Exon 51 in a Humanized Duchenne Muscular Dystrophy Mouse Model Abolishes Ventricular Arrhythmia Predisposition.” Circ Genom Precis Med 18, no. 3 (June 2025): e004867. https://doi.org/10.1161/CIRCGEN.124.004867.

Perelli RM, Sitton MJ, Bohning JD, Pickar-Oliver A, McCullough KT, Moya-Mendez ME, et al. Deletion of Exon 51 in a Humanized Duchenne Muscular Dystrophy Mouse Model Abolishes Ventricular Arrhythmia Predisposition. Circ Genom Precis Med. 2025 Jun;18(3):e004867.

Perelli, Robin M., et al. “Deletion of Exon 51 in a Humanized Duchenne Muscular Dystrophy Mouse Model Abolishes Ventricular Arrhythmia Predisposition.” Circ Genom Precis Med, vol. 18, no. 3, June 2025, p. e004867. Pubmed, doi:10.1161/CIRCGEN.124.004867.

Perelli RM, Sitton MJ, Bohning JD, Pickar-Oliver A, McCullough KT, Moya-Mendez ME, Zheng S, Daniels H, Devlin G, Asokan A, Gersbach CA, Landstrom AP. Deletion of Exon 51 in a Humanized Duchenne Muscular Dystrophy Mouse Model Abolishes Ventricular Arrhythmia Predisposition. Circ Genom Precis Med. 2025 Jun;18(3):e004867.