Figure 3 | Scientific Reports

Figure 3

From: A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss

Figure 3The alternative text for this image may have been generated using AI.

The POU4F3 c.982A>G mutation altered the subcellular localization of transcription factor POU4F3. Nuclei stained with DAPI (blue) and POU4F3 detected by Anti-DYKDDDDK-Tag antibody (red) were visualized by confocal microscopy. The white arrows indicate POU4F3 outside the nuclei.

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