GJB2 Gene Mutations in Childhood Deafness
Author:
Publisher
Informa UK Limited
Subject
Otorhinolaryngology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/000164800750000766
Reference13 articles.
1. Genetic Epidemiology of Hearing Impairment
2. Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations
3. Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
4. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
5. Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene
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1. Genetic etiology of non-syndromic hearing loss in Latin America;Human Genetics;2021-10-15
2. Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss;Human Genetics;2021-10-01
3. Systematic Review of Pathogenic GJB2 Variants in the Latino Population;Otology & Neurotology;2020-02
4. GJB2 and GJB6 mutations are an infrequent cause of autosomal-recessive nonsyndromic hearing loss in residents of Mexico;International Journal of Pediatric Otorhinolaryngology;2014-12
5. Neural Coding of Sound with Cochlear Damage;Noise-Induced Hearing Loss;2011-09-13
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