Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene.

Zdeněk ČadaDana Šafka BrožkováZuzana BalatkováPavlína PlevováDagmar RaškováJana LaštůvkováRudolf ČernýVeronika BandúrováVladimír KouckýSilvie HrubáMartin KomarcJán JenčíkSimona Poisson MarkováJan PlzákJan KluhPavel Seeman

Published in: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery (2019)

Moderate sensorineural hearing loss is typical for DFNB16-associated hearing loss and there are no significant differences in audiological phenotypes among different types of mutations affecting STRC.

Keyphrases

hearing loss
high intensity
copy number
genome wide identification
transcription factor