DFNB59 Gene Mutation Screening Using PCR-SSCP/HA Technique in Non-syndromic Genetic Hearing Loss in Bushehr Province

DFNB59 Gene Mutation Screening Using PCR-SSCP/HA Technique in Non-syndromic Genetic Hearing Loss in Bushehr Province

Background: Hearing impairment (HI) is the most prevalent Neurosensory disorder which is heterogenous and can also occur due to environmental causes. The majority of hearing deficiencies are of genetic origin affecting about 60% of the HI cases. A novel gene DFNB59 encodes pejvakin has been recently...

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Bibliographic Details
Main Authors: Fatemeh Azadegan Dehkordi, Effat Farrokhi, Mostafa Montazer Zohouri, Gholamreza Mobini, Maryam Taherzadeh, Marzieh Raiesi, Gol andam Banitalebi, Somaieh Raiesi, Mehdi Banitalebi, Morteza Hashemzadeh Chaleshtari
Format: Article
Language:English
Published: Bushehr University of Medical Sciences 2010-09-01
Series:Iranian South Medical Journal
Subjects:
hearing impairment
pejvakin
DFNB59 gene
polymorphism
single- strand conformation polymorphism
hetero duplex analysis
Online Access:http://ismj.bpums.ac.ir/browse.php?a_code=A-10-3-194&slc_lang=en&sid=1

Internet

http://ismj.bpums.ac.ir/browse.php?a_code=A-10-3-194&slc_lang=en&sid=1

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