Information Journal Paper
APA:
Copy. (2019). 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, 23(1), 20-26. SID. https://sid.ir/paper/767884/en
Vancouver:
Copy. 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[Internet]. 2019;23(1):20-26. Available from: https://sid.ir/paper/767884/en
IEEE:
Copy, “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, vol. 23, no. 1, pp. 20–26, 2019, [Online]. Available: https://sid.ir/paper/767884/en