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About this Neuroscience article
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 by Azadegan-Dehkordi, Fatemeh ;Bahrami, Tayyebe ;Shirzad, Maryam ;Karbasi, Gelareh ;Yazdanpanahi, Nasrin ;Farrokhi, Effat ;Koohiyan, Mahbobeh ;Tabatabaiefar, Mohammad Amin ;Hashemzadeh-Chaleshtori, Morteza is a Neuroscience article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Neuroscience.
- Author
- Azadegan-Dehkordi, Fatemeh ;Bahrami, Tayyebe ;Shirzad, Maryam ;Karbasi, Gelareh ;Yazdanpanahi, Nasrin ;Farrokhi, Effat ;Koohiyan, Mahbobeh ;Tabatabaiefar, Mohammad Amin ;Hashemzadeh-Chaleshtori, Morteza
- Publisher
- The Korean Audiological Society; Korean Audiological Society (ISSN 2384-1621)
- Published
- 2019
- Field
- Neuroscience (Life Sciences)