Audiological features in Serbian patients with hearing impairment identified with c.35delG in the GJB2 gene

Audiological features in Serbian patients with hearing impairment identified with c.35delG in the GJB2 gene

Introduction/Objective. Hearing impairment is the most common sensorineural disorder with an incidence of 1/700–1000 newborns. Variants in the GJB2 gene are the major cause of autosomal recessive nonsyndromic sensorineural hearing loss (ARNSHL). The degree of hearing impairment in patients with dete...

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Bibliographic Details
Main Authors: Dobrić Bojana, Radivojević Danijela, Ječmenica Jovana, Neocleous Vassos, Fanis Pavlos, Phylactou Leonidas A., Đurišić Marina
Format: Article
Language:English
Published: Serbian Medical Society 2021-01-01
Series:Srpski Arhiv za Celokupno Lekarstvo
Subjects:
hearing impairment
gjb2 gene
c.35delg variant
audiological features
Online Access:http://www.doiserbia.nb.rs/img/doi/0370-8179/2021/0370-81792100098D.pdf

Internet

http://www.doiserbia.nb.rs/img/doi/0370-8179/2021/0370-81792100098D.pdf

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