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. 2024 Aug 9;14:19. doi: 10.1186/s13395-024-00350-6

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© The Author(s) 2024

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — Body and muscle mass of WT and dysferlin-deficient BLA/J mice aged 10 months, without and with dexamethasone (Dex) treatment. A Body mass measured at sampling, and B quadriceps (quad), C soleus, and D extensor digitorum longus (EDL) muscle mass normalised to body mass (mg/gBM). Data were analysed by two-way ANOVA: **** BLA/J (± Dex) vs WT (± Dex) (p < 0.0001, strain effect); # Dex-treated vs. untreated (p < 0.05, treatment effect); ^^ BLA/J + Dex vs WT + Dex (p < 0.01, strain/treatment interaction effect). Data are presented as mean ± SD (n = 8–9)