Twenty years of clinical studies of GJB2-linked hearing loss in Russia
Author:
Publisher
Media Sphere Publishing Group
Subject
Otorhinolaryngology
Reference23 articles.
1. Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
2. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
3. Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene
4. Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss
5. Non-syndromic hearing impairment: gene linkage and cloning
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1. Assessment of the risk of hearing loss in children with cystic fibrosis;Russian Bulletin of Otorhinolaryngology;2024
2. Audiological Evidence of Frequent Hereditary Mild, Moderate and Moderate-to-Severe Hearing Loss;Journal of Personalized Medicine;2022-11-04
3. Identification of Pathogenic Variant Burden and Selection of Optimal Diagnostic Method Is a Way to Improve Carrier Screening for Autosomal Recessive Diseases;Journal of Personalized Medicine;2022-07-12
4. The role of molecular-biological characteristics of the organism in the development of professional sensorineural hearing loss;Russian Journal of Occupational Health and Industrial Ecology;2022-06-25
5. Genetic Variant c.245A>G (p.Asn82Ser) in GIPC3 Gene Is a Frequent Cause of Hereditary Nonsyndromic Sensorineural Hearing Loss in Chuvash Population;Genes;2021-05-27
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