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

In a previous study, we identified a novel missense mutation, , in the GJC3 gene encoding () from patients with hearing loss. The functional alteration of caused by the mutant of GJC3 gene, however, remains unclear. | Functional analysis of a nonsyndromic hearing loss-associated mutation in the transmembrane II domain of the GJC3 gene

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