Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.
Sign Up to like & getrecommendations! Published in 2017 at "International journal of pediatric otorhinolaryngology"
DOI: 10.1016/j.ijporl.2017.08.006
Abstract: OBJECTIVES The genetics of sensorineural hearing loss is characterized by a high degree of heterogeneity. Despite this heterogeneity, DNA variants found within SLC26A4 have been reported to be the second most common contributor after those… read more here.
Keywords: hearing loss; related hearing; loss; novel pathogenic ... See more keywords