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Fig. 2 | BMC Genomics

Fig. 2

From: A murine model for the del(GJB6-D13S1830) deletion recapitulating the phenotype of human DFNB1 hearing impairment: generation and functional and histopathological study

Fig. 2

Auditory phenotype of P30 Dfnb1em274 HOM mice. a ABR in response to click stimulus at different level from 90 to 30 dB SPL, in WT, HET and HOM Dfnb1em274 mice. Latin numbers (I-V) indicate the standard ABR peaks. b Scheme showing the main neural centers in the auditory pathway and their correspondence with the ABR wave peaks (AN (I): auditory nerve; CN (II), cochlear nucleus; SOC (III): superior olivary complex; LL (IV): lateral lemniscus; IC (V), inferior colliculus; NLL: Lateral lemniscus nuclei; MGB, medial geniculate body; SC, superior colliculus; TL, temporal lobe; AC, auditory cortex. c, d ABR thresholds (in dB SPL) in response to click (c) and 4–40 kHz pure tones (d) in WT (white), HET (grey) and HOM (black) Dfnb1em274 mice. Statistically significant differences in click and 4, 8 and 16 kHz thresholds were found between WT and HOM mutant mice. (e) Input–output curves (latency/intensity and amplitude/intensity) for ABR peak I and (f) wave interpeak latencies I-II, II-IV and I-IV in WT and HET mutant mice

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