Prevalence Study of GJB2 Gene Mutations in Iranian Ethnics

Prevalence Study of GJB2 Gene Mutations in Iranian Ethnics

Objective: Hereditary hearing loss (HHL) is a very common disorder. When inherited in an autosomal recessive manner, it typically presents as an isolated finding. Interestingly and unexpectedly, in spite of extreme heterogeneity, mutations in one gene, GJB2, are the most common cause of congenital s...

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Bibliographic Details
Main Authors: Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Noushin Nik-Zaat, Khadijeh Jalalvand, Yaser Riaz-el Hosseini, Yousef Shafeghati, Sanaz Arzhangi, Khalil Javan, Hosein Najmabadi
Format: Article
Language:fas
Published: University of Social Welfare and Rehabilitation Sciences 2007-10-01
Series:Journal of Rehabilitation
Subjects:
GJB2 mutations
35delG
Iran
Hereditary hearing loss
Autosomal inheritance
Online Access:http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-188&slc_lang=en&sid=1

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http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-188&slc_lang=en&sid=1

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