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- 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
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