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-Reference-Cited by-同舟云学术

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

Published:2019-01-10 Issue:1 Volume:23 Page:20-26
ISSN:2384-1621
Container-title:Journal of Audiology and Otology
language:en
Short-container-title:J Audiol Otol

Author:

Azadegan-Dehkordi Fatemeh,Bahrami Tayyebe,Shirzad Maryam,Karbasi Gelareh,Yazdanpanahi Nasrin,Farrokhi Effat,Koohiyan Mahbobeh,Tabatabaiefar Mohammad Amin,Hashemzadeh-Chaleshtori Morteza

Funder

Shahrekord University of Medical Sciences

Publisher

The Korean Audiological Society

Subject

Speech and Hearing,Sensory Systems

Link

http://ejao.org/upload/pdf/jao-2018-00185.pdf

Reference30 articles.

1. Compound Heterozygosity for Two NovelSLC26A4Mutations in a Large Iranian Pedigree with Pendred Syndrome

2. A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss

3. Unresolved questions regarding human hereditary deafness