DFNB59 Gene Mutations and its Association with Deafness in Schoolchildren in Kohgilooyeh & Boyerahmad Province

DFNB59 Gene Mutations and its Association with Deafness in Schoolchildren in Kohgilooyeh & Boyerahmad Province

Introduction & Objective: Hearing loss is a common disease affecting millions of people worldwide. Hearing loss can be caused due to genetic or environmental factors or even both. The genetic of hearing defect is highly heterogeneous and more than 100 genes are predicted to cause this disorder i...

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Bibliographic Details
Main Authors:	M Taherzadeh Ghahfarrokhi, E Farrokhi, A Shirmardi, S Ghasemi, M Abolhasani, F Azadegan, S Reisi, M Reisi, G Banitalebi, M Hashemzadeh Chaleshtori
Format:	Article
Language:	fas
Published:	Yasuj University Of Medical Sciences 2010-01-01
Series:	Armaghane Danesh Bimonthly Journal
Subjects:	Deafness DFNB59 PCR-SSCP Heteroduplex Analysis.
Online Access:	http://armaghanj.yums.ac.ir/browse.php?a_code=A-10-1-420&slc_lang=en&sid=1

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