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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 2019 Jun 27 DOI: https://doi.org/10.7874/jao.2019.00059
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Citations to this article as recorded by
 Identification of GJB2 Variants in 75 Unrelated Iranian Autosomal Recessive Non-syndromic Hearing Loss Patients
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Journal of Human Genetics and Genomics.2022;[Epub] CrossRef An update on autosomal recessive hearing loss and loci involved in it
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Indian Journal of Otology.2022; 28(1): 6. CrossRef Molecular alteration in the Gap Junction Beta 2 (GJB2) gene associated with non-syndromic sensorineural hearing impairment
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Intractable & Rare Diseases Research.2021; 10(1): 31. CrossRef GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran
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International Journal of Pediatric Otorhinolaryngology.2020; 129: 109756. CrossRef Identification and clinical implications of a novel pathogenic variant in the GJB2 gene causes autosomal recessive non-syndromic hearing loss in a consanguineous Iranian family
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Intractable & Rare Diseases Research.2020; 9(1): 30. CrossRef Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation
Chang Guo, Sha-Sha Huang, Yong-Yi Yuan, Ying Zhou, Ning Wang, Dong-Yang Kang, Su-Yan Yang, Xin Zhang, Xue Gao, Pu Dai
Neural Plasticity.2020; 2020: 1. CrossRef
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