Fig. 2From: A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese familyPure‑tone audiograms of the family members. A Affected individuals IV:1, V:2, and V:9. B Unaffected individuals IV:2, V:4, V:6, V:10, V:14, and VI:8. R, Right; L, Left; y, yearsBack to article page