 |
| CrossRef Text and Data Mining |
| Result of CrossRef Text and Data Mining Search is the related articles with entitled article. If you click link1 or link2 you will be able to reach the full text site of selected articles; however, some links do not show the full text immediately at now. If you click CrossRef Text and Data Mining Download icon, you will be able to get whole list of articles from literature included in CrossRef Text and Data Mining. |
| Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran |
| Fatemeh Azadegan-Dehkordi, Tayyebe Bahrami, Maryam Shirzad, Gelareh Karbasi, Nasrin Yazdanpanahi, Effat Farrokhi, Mahbobeh Koohiyan, Mohammad Amin Tabatabaiefar, Morteza Hashemzadeh-Chaleshtori |
|
J Audiol Otol. 2019;23(1):20-26. Published online December 7, 2018 DOI: https://doi.org/10.7874/jao.2018.00185 |
|
Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran Journal of Audiology and Otology. 2019;23(1):20-26  GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran Journal of Clinical Laboratory Analysis. 2021;35(11): GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss Human Mutation. 2002;19(5):572-572 Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness International Journal of Pediatric Otorhinolaryngology. 2007;71(6):869-873 Connexin 26 (GJB2) Gene Mutations Linked With Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in Iraqi Population. . 2021; Connexin 26 (GJB2) Gene Mutations Linked With Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in Iraqi Population . 2021; GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation International Journal of Pediatric Otorhinolaryngology. 2007;71(8):1239-1245 Identification of GJB2 Variants in 75 Unrelated Iranian Autosomal Recessive Non-syndromic Hearing Loss Patients Journal of Human Genetics and Genomics. 2022;4(1): Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran International Journal of Pediatric Otorhinolaryngology. 2015;79(11):1892-1895 Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: Assessment of GJB4, GJA1, and GJC3 International Journal of Pediatric Otorhinolaryngology. 2013;77(2):189-193 |
