Relative Frequency of 35delG Mutation in GJB2 Gene in Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) Patients in Kerman Population
Congenital hearing loss with many genetic and environmental causes affects 1 in 1000 newborns. Mutations in the GJB2(Gap Junction Beta-2) gene encoding the gap junction protein connexin 26 have been established as the main cause of autosomal recessive non-syndromic hearing loss. The aim of this stud...
Main Authors: | , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Kerman University of Medical Sciences
2004-07-01
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Series: | Journal of Kerman University of Medical Sciences |
Subjects: | |
Online Access: | https://jkmu.kmu.ac.ir/article_32762_50837385184f043fc057a0efcda79b20.pdf |