"Deafness –Associated Connexin 26 Gene (GJB2) Mutations in Iranian Population"

"Deafness –Associated Connexin 26 Gene (GJB2) Mutations in Iranian Population"

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Mutations in the GJB2 gene at the DFNB1 locus on chromosome 13q12 are associated with autosomal recessive non syndromic hearing loss (ARNSHL) in many populations. A single mutation, at position 35 (35delG) accounts for approximately 30-63% of mutations in white populations with a carrier frequency o...

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Bibliographic Details
Main Authors: M Hashemzadeh Chaleshtori, DD Farhud, R Taylor, V Hadavi, MA Patton, AR Afzal
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2002-09-01
Series:Iranian Journal of Public Health
Subjects:
Autosomal recessive non syndromic hearing loss
Online Access:http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/293.pdf&manuscript_id=293

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