Fig. 1
From: The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report
a Pedigree of the family with a de novo mutation causing hearing loss in the proband (filled circle). b Auditory brainstem response (ABR) of the proband (III-1) at 1 month after birth. c Temporal bone computed tomogram of the inner ear (III-1) d Pure-tone audiogram of the father (II-1), mother (II-2), and proband (III-1). Red and blue indicate thresholds for the right and left ears, respectively. Solid and dashed lines refer to air- and bone-conduction, respectively