Missense Variant of Endoplasmic Reticulum Region of <i>WFS1</i> Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype

<div>Audiological and imaging evaluation. (a) The PTA of the right and left ears of representative affected family members and a normal family member. (b) Internal auditory canal MRI and CT scans of the temporal bone in the proband (III-2). The first line contains two CT images of the proband’s bilateral temporal bones. The second row contains two MR images of the proband’s bilateral internal auditory canals.</div>

BioMed Research International

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Figure 2: Missense Variant of Endoplasmic Reticulum Region of <i>WFS1</i> Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype 

BioMed Research International

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype

Figure 2