A Missense <i>POU4F3</i> Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities

<div>Sanger sequencing of wild-type (WT) and mutant (MUT) POU4F3. Red arrow indicates the position of the c.602T&gt;C variant in <i>POU4F3</i>.</div>

BioMed Research International

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Figure 1

Figure 1: A Missense <i>POU4F3</i> Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities 

Figure 1 | A Missense POU4F3 Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities 