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Autosomal Recessive and Sporadic Non Syndromic Hearing Loss and the Incidence of Cx26 Mutations in a Province of Iran

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Despite the enormous heterogeneity of genetic hearing loss, mutations in the GJB2 (connexin 26) gene located on "DFNB1" locus (13q12) account for up to 50% of cases of autosomal recessive non-syndromic hearing loss (ARNSHL) in some populations. This study describes the analysis of 100 auto...

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Main Authors: M Hashemzadeh Chaleshtori (Author), M Montazer Zohour (Author), L Hoghooghi Rad (Author), H Pour-Jafari (Author), DD Farhud (Author), M Dolati (Author), K Safa Chaleshtori (Author), R Sasanfar (Author), A Hosseinipour (Author), L Andonian (Author), A Tolouei (Author), M Ghadami (Author), MA Patton (Author)
Format: Book
Published: Tehran University of Medical Sciences, 2006-05-01T00:00:00Z.
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