# Correction: A novel mouse model of Duchenne muscular dystrophy carrying a multi-exonic Dmd deletion exhibits progressive muscular dystrophy and early-onset cardiomyopathy

**Authors:** Tatianna Wai, Ying Wong, Abdalla Ahmed, Grace Yang, Eleonora Maino, Sydney Steiman, Elzbieta Hyatt, Parry Chan, Kyle Lindsay, Nicole Wong, Diane Golebiowski, Joel Schneider, Paul Delgado-Olguín, Evgueni A. Ivakine, Ronald D. Cohn

PMC · DOI: 10.1242/dmm.052372 · Disease Models & Mechanisms · 2025-04-04

## Full-text entities

- **Genes:** Dmd (dystrophin, muscular dystrophy) [NCBI Gene 13405] {aka DXSmh7, DXSmh9, Dp427, Dp71, dys, mdx}
- **Diseases:** muscular dystrophy (MESH:D009136), Duchenne muscular dystrophy (MESH:D020388), cardiomyopathy (MESH:D009202)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

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Source: https://tomesphere.com/paper/PMC11993248