A new dystrophin-deficient rat model mirroring exon skipping…

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A new dystrophin-deficient rat model mirroring exon skipping in patients with DMD exon 45 deletions

Article 2026 EN Gold

ABSTRACT Mutations in the dystrophin (DMD) gene can cause a spectrum of muscle-wasting disorders ranging from the milder Becker muscular dystrophy (BMD) to the more severe Duchenne muscular dystrophy (DMD). Among these, exon 45 deletion is the most frequently reported single exon deletion in DMD patients worldwide. In this study, we generated a novel rat model with an exon 45 deletion using CRISPR…

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14 authors
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1 Tao Wang Inserm (FR) Université Paris-Saclay (FR) +2 —
2 Cynthia Daoud Inserm (FR) Université Paris-Saclay (FR) +2 —
3 Auriane Dubois Inserm (FR) Université Paris-Saclay (FR) +2 —
4 Guillaume Corre Inserm (FR) Université Paris-Saclay (FR) +2
5 Jessica Bellec Inserm (FR) Université Paris-Saclay (FR) +2 —
6 Matteo Bovolenta Inserm (FR) Université Paris-Saclay (FR) +2
7 Louise Philidet Inserm (FR) Université Paris-Saclay (FR) +2 —
8 Alan Dorval Inserm (FR) Université Paris-Saclay (FR) +2 —
9 Nathalie Bourg Inserm (FR) Université Paris-Saclay (FR) +2
10 Carinne Roudaut Inserm (FR) Université Paris-Saclay (FR) +2
11 Sonia Albini Inserm (FR) Université Paris-Saclay (FR) +2
12 Ganesh Warthi Inserm (FR) Université Paris-Saclay (FR) +2
13 Abbass Jaber Corresponding Inserm (FR) Université Paris-Saclay (FR) +2
14 Isabelle Richard Corresponding Inserm (FR) Université Paris-Saclay (FR) +2
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