Evaluation of GJB2 and GJB6 Mutations in Patients Afflicted with Non-syndromic Hearing Loss

Evaluation of GJB2 and GJB6 Mutations in Patients Afflicted with Non-syndromic Hearing Loss

Background Non-syndromic hearing loss (NSHL) is assumed as one of the highly prevalent congenital defects in the world. In this regard, gap junction protein beta 2(GJB2), and gap junction protein beta 6(GJB6) mutations are considered as the leading congenital causes of deafness. The present study ai...

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Bibliographic Details
Main Authors: Seyed Hamid Reza Abtahi, Ali Malekzadeh, Saeed Soheilipour, Mansour Salehi, Roya Taleban, Reyhaneh Rabieian, Mohammad Moafi
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2019-02-01
Series:International Journal of Pediatrics
Subjects:
hearing loss
GJB2
GJB6
Mutation
Online Access:http://ijp.mums.ac.ir/article_11447_48d7dbaa820ef662b43289339aa49c4b.pdf

Internet

http://ijp.mums.ac.ir/article_11447_48d7dbaa820ef662b43289339aa49c4b.pdf

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