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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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Egile Nagusiak: M Hashemzadeh Chaleshtori (Egilea), DD Farhud (Egilea), AH Crosby (Egilea), E Farrokhi (Egilea), H Pour Jafari (Egilea), K Ghatreh Samani (Egilea), K Safa Chaleshtori (Egilea), M Kasiri (Egilea), M Shahrani (Egilea), GR Mobini (Egilea), M Mansouri (Egilea), D Modarresinia (Egilea), M Jafari (Egilea)
Formatua: Liburua
Argitaratua: Tehran University of Medical Sciences, 2008-09-01T00:00:00Z.
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