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| Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations |
| Mahbobeh Koohiyan, Fatemeh Azadegan-Dehkordi, Farideh Koohian, Morteza Hashemzadeh-Chaleshtori |
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J Audiol Otol. 2019;23(4):175-180. Published online June 27, 2019 DOI: https://doi.org/10.7874/jao.2019.00059 |
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Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations Journal of Audiology and Otology. 2019;23(4):175-180  GJB2
‐related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations Annals of Human Genetics. 2019;84(2):107-113 Update of the Spectrum ofGJB2Mutations in 107 Patients with Nonsyndromic Hearing Loss in the Fujian Population of China Annals of Human Genetics. 2014;78(3):235-242 Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria Human Genetics. 2002;111(2):145-153 An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review International Journal of Pediatric Otorhinolaryngology. 2019;119:136-140 The frequency of GJB2 and GJB6 mutations in the New York State newborn population: feasibility of genetic screening for hearing defects Clinical Genetics. 2004;65(4):338-342 GJB2 mutation spectrum in the Taiwanese population and genotype–phenotype comparisons in patients with hearing loss carrying GJB2 c.109G>A and c.235delC mutations Hearing Research. 2022;413:108135 Update of spectrum c.35delG and c.‐23+1G>A mutations on the
GJB2
gene in individuals with autosomal recessive nonsyndromic hearing loss Annals of Human Genetics. 2018;83(1):1-10 High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India International Journal of Pediatric Otorhinolaryngology. 2009;73(3):437-443 GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysis Clinical Genetics. 2005;68(6):554-557 |
