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Fig. 1

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Publication: Chen et al., 2026 - GJB2 c.109G > A mutation activating IFI27-mediated mitochondrial apoptosis pathway leading to hereditary non-syndromic hearing loss
All Figures: Figures for Chen et al., 2026

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Fig. 1

Gene structure and common mutation sites of GJB2. The data is derived from 1,199 samples collected by our hospital from January to September 2023. GJB2 deafness gene mutations accounted for 85% of all detected mutation types, among which the c.109G > A mutation was the most common. Different colors are only for distinguishing different mutations.

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