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

<div>Pedigree of the family with autosomal dominant hearing impairment. Proband: arrow; affected individuals: gray symbols; males: squares; females: circles; participants clinically and genetically examined: red box.</div>

BioMed Research International

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Figure 1

Figure 1: 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 1