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Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation.

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Academic year: 2017

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Figure 2. The haplotypes around c.211delC mutation of six families constructed using SNPs are shown
Figure 3. Overlapping audiograms from the better ear for each genotype. In cases of W276S, c.211delC, or V230E, light colored audiograms (green, blue, red) were from individuals aged 19 and under
Table 2 summarizes clinical characteristics including hearing threshold, severity, onset age (age of awareness), progressiveness of hearing loss, and vestibular symptoms

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