Study of Cx 26 gene mutations in patients with non-syndromic sensorineural hearing loss

@inproceedings{Onsori2018StudyOC,
  title={Study of Cx 26 gene mutations in patients with non-syndromic sensorineural hearing loss},
  author={Onsori},
  year={2018}
}
Background: Non-syndromic sensorineural hearing loss (NSHL) is the most common sensory disorder worldwide and more than 100 genetic loci have been identified in NSHL so far. Mutations in the CX26 (GJB2) gene at the DFNB1 locus on chromosome 13q12 are associated with autosomal recessive non-syndromic hearing loss in a variety of populations. The purpose of this study was to investigate the CX26 gene mutations in patients with NSHL. Materials and Methods: In this descriptive laboratory study, 50… CONTINUE READING

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