Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene.

Int J Med Sci · 2017 · PMC5370287 · PMID 28367085

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highly significantno p-value reported

After unpaired t-test analysis, both CQ (p=0.0224 and p=0.0162, respectively) and MG132 treatment (p=0.0335 and p=0.0013, respectively) were highly significant than no-treatment (control) at the treatment 24 and 48 hours group.

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