Journal of Inflammatory Diseases
The Official Journal of Qazvin University of Medical Sciences
A case report of non-syndromic sensorineural hearing loss with a compound heterozygous mutation (35delG/del120E) in the GJB2 gene
Abstract
Copyright
© 2024, Journal of Inflammatory Diseases. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.
Similar Articles
Frequency of Connexin26 Gene Mutations in Autosomal Recessive Non-syndromic Deafness in Kermanshah(2002-4)
Mahdieh N, Nishimura C, Ali-Madadi K, Yazdan Y, Kazemi S, et al. Frequency of Connexin26 Gene Mutations in Autosomal Recessive Non-syndromic Deafness in Kermanshah(2002-4). J Kermanshah Univ Med Sci. 2005;9(2):e81569. doi:
Prevalence of GJB2 mutations among patients with autosomal recessive non syndromic hearing loss in Sistan and Baloochestan province
Naghavi A, Nishimura K, Kahrizi K, Riazalhosseini Y, Suraki Aliabadib H, et al. Prevalence of GJB2 mutations among patients with autosomal recessive non syndromic hearing loss in Sistan and Baloochestan province. Zahedan J Res Med Sci. 2005;7(2):e94965. doi:
Frequency of Hearing Impairment among Full-term Newborns in Yazd, Iran
Islami Z, Baradaranfar M, Mehrparvar A, Mollasadeghi A, Mostaghaci M, et al. Frequency of Hearing Impairment among Full-term Newborns in Yazd, Iran. Inn J Pediatr. 2013;23(3):. doi:
Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss
Talebi F, Ghanbari Mardasi F, Mohammadi Asl J. Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss. Zahedan J Res Med Sci. 2016;18(10):e4256. doi: https://doi.org/10.17795/zjrms-4256
The contribution of autosomaul recessive non-syndromic deafness to DFNB59 mutations (Pejvakin)
Abolhasani M, Farrokhi E, Noorbakhsh M, Taherzadeh M, Azadegan F, et al. The contribution of autosomaul recessive non-syndromic deafness to DFNB59 mutations (Pejvakin). Zahedan J Res Med Sci. 2010;12(3):e94295. doi:
- Scopus by DOI: 0
Last Update: 1 month ago
- Scopus by Title: 0
Last Update: 1 month ago
- Scopus by Title (Ref): 0
Last Update: 1 month ago
- CrossRef: 0
Last Update: 2 days ago
Ordering Reprints
Articles are published under the Creative Commons license stated on each article. No permission or royalty fee is required for uses permitted by that license. CCC handles optional bulk and customized reprint orders. Any quotation covers production and delivery services only, not copyright permission. > Request Reprints from CCC