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Molecular Pathology of 6 Novel GJB2 Allelic Variants Detected in Familial and Sporadic Iranian Non Syndromic Hearing Loss Cases

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"nBackground: Mutations of GJB2 gene encoding connexion 26 are the most common cause of hearing loss in many popula­tions. A very wide spectrum of GJB2 gene mutations associated with hearing loss have been detected but pathogenic role has been tested only for a part of them. In this stu...

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Main Authors: M Hashemzadeh Chaleshtori (Author), DD Farhud (Author), AH Crosby (Author), E Farrokhi (Author), H Pour Jafari (Author), K Ghatreh Samani (Author), K Safa Chaleshtori (Author), M Kasiri (Author), M Shahrani (Author), GR Mobini (Author), M Mansouri (Author), D Modarresinia (Author), M Jafari (Author)
Format: Book
Published: Tehran University of Medical Sciences, 2008-09-01T00:00:00Z.
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