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 2018 Dec 7     DOI: https://doi.org/10.7874/jao.2018.00185
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An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review
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International Journal of Pediatric Otorhinolaryngo.2019; 119: 136.     CrossRef