Connecxin 26 Gene Mutations in Non-Syndromic Hearing Loss in Hamadan Province

Connecxin 26 Gene Mutations in Non-Syndromic Hearing Loss in Hamadan Province

Introduction & Objective : Hearing loss is the most prevalent form of sensory impairment in humans, affecting approximately one in 1000 infants. In more than half of the cases, the deafness is inherited, and about 80% of hereditary deafness transmitted by autosomal recessive pattern. In heredita...

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Bibliographic Details
Main Authors: Yousef Shafeghati, Ahmad Ebrahimi, Marzieh Mohseni, Farzaneh Ostadi, Halleh Habibi, Hamid Poujafari, R.J.H Esmith, Hosein Najmabadi
Format: Article
Language:fas
Published: Hamadan University of Medical Sciences 2006-03-01
Series:پزشکی بالینی ابن سینا
Subjects:
gene connecxin 26
hearing loss
hereditary
non-syndromic
mutation
Online Access:http://sjh.umsha.ac.ir/article-1-513-en.html

Internet

http://sjh.umsha.ac.ir/article-1-513-en.html

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