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Frequencies of Mutations in the Connexin 26 Gene (GJB2) in Two Populations of Iran (Tehran and Tabriz)

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While hearing loss has been considered to be a very heterogeneous disorder, mutations in Gap junction beta 2 (GJB2) gene encoding Connexin 26 (Cx26) protein are the major cause of autosomal recessive and sporadic non-syndromic deafness in many populations. In this study, we have investigated the pre...

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Bibliographic Details
Main Authors: M Hashemzadeh Chaleshtori (Author), L Hoghooghi Rad (Author), M Dolati (Author), R Sasanfar (Author), A Hoseinipour (Author), M Montazer Zohour (Author), H Pourjafari (Author), A Tolooi (Author), M Ghadami (Author), DD Farhud (Author), MA Patton (Author)
Format: Book
Published: Tehran University of Medical Sciences, 2005-03-01T00:00:00Z.
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3rd Floor Main Library

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