Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort


Creative Commons License

Cengiz F. B., Yilmazer R., Olgun L., SENNAROĞLU L., KİRAZLI T., Alper H., ...Daha Fazla

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, cilt.101, ss.167-171, 2017 (SCI-Expanded) identifier identifier identifier

Özet

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 of GJB2 in many populations.