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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
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   Crossref logo
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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   Crossref logo
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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   Crossref logo
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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   Crossref logo
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<i>GJB2</i> Gene Related Nonsyndromic Hearing Loss in Mazandaran Province, North of Iran
Open Journal of Genetics. 2020;10(03):51-63   Crossref logo
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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. 2020;108135   Crossref logo
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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   Crossref logo
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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   Crossref logo
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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   Crossref logo
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GJB2 gene mutations in Slovak hearing-impaired patients of Caucasian origin: spectrum, frequencies and SNP analysis
Clinical Genetics. 2005;68(6):554-557   Crossref logo
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