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"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 (Author), DD Farhud (Author), R Taylor (Author), V Hadavi (Author), MA Patton (Author), AR Afzal (Author)
Format:	Book
Published:	Tehran University of Medical Sciences, 2002-12-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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