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Figure 3 | Orphanet Journal of Rare Diseases

Figure 3

From: High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss

Figure 3

Comparison of hearing levels between individuals homozygous for p.P240L and those with other homozygous mutations. A: Overlapping audiograms of subjects with homozygous p.P240L mutations. B: Overlapping audiograms of the subjects with non-p.P240L homozygous mutations. The subjects with homozygous p.P240L mutations tended to have more severe hearing loss at lower frequencies.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172