Fig. 2From: Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case reportA mutation in WFS1 identified using whole-exome sequencing. a Sanger sequencing traces of subjects 30–11, 30–12, 30–21, and 30–22. b Multiple sequence alignment of WFS1 among different species. p.S807 is well preserved among various speciesBack to article page