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. 2024 Nov 1;56(11):2423–2435. doi: 10.1038/s12276-024-01338-4

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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/.

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Fig. 1 — a Overall appearance of Myh1^+/+, Myh1^+/−, and Myh1^−/− mice at postnatal Day 30. b Body weights of the Myh1^+/+, Myh1^+/−, and Myh1^−/− mice. c Tone-pip ABR thresholds, d click ABR thresholds, and e ABR I/O functions of the Myh1^+/+, Myh1^+/−, and Myh1^−/− mice at postnatal Day 30. f DPOAE thresholds and g DPOAE I/O functions at 6 kHz and h 30 kHz. b–h Myh1^+/+ (black, n = 5), Myh1^+/− (blue, n = 7), and Myh1^−/− (red, n = 7) mice. The data are presented as the means ± SEMs. Statistical comparisons were performed using two-way ANOVA with Bonferroni correction for multiple comparisons in (b–h). **P < 0.01 and ***P < 0.001.