Compound heterozygosity of the functionally null Cdh23(v-ngt) and hypomorphic Cdh23(ahl) alleles leads to early-onset progressive hearing loss in mice.

Exp Anim · 2013 · PMC4160959 · PMID 24172198

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did not reach statistical significanceno p-value reported

For ABR thresholds in response to stimuli at 4 kHz, mean differences were detected between Cdh23 ahl/ahl and Cdh23 v-ngt/ahl mice at several time points, but they did not reach statistical significance.

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