Spectrum of Gjb2 Gene Mutations in Nonsyndromic Autosomal Recessive Deaf Patients in Yazd

Spectrum of Gjb2 Gene Mutations in Nonsyndromic Autosomal Recessive Deaf Patients in Yazd

Introduction: Hearing loss is the most common sensory neural defect in humans, affecting 1 in 1000 neonates, with over half of these cases predicted to be hereditary in nature. Most hereditary hearing loss is inherited in a recessive fashion, accounting for approximately 80 % of non-syndromic hearin...

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Bibliographic Details
Main Authors: H Najmabadi, R Smith, MK Javan, M Abhaji, N Bazazzadegan, A Dehghani, Y Riazzalhoseini, K Kahrizi, M Mirab, M Seifati, H Khodaie, M Moghannibashi
Format: Article
Language:fas
Published: Shahid Sadoughi University of Medical Sciences 2005-10-01
Series:Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd
Subjects:
GJB2
35delG
312del14
Autosomal recessive non-syndromic deafness
population of Yazd.
Online Access:http://jssu.ssu.ac.ir/browse.php?a_id=704&slc_lang=en&sid=1&ftxt=1

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http://jssu.ssu.ac.ir/browse.php?a_id=704&slc_lang=en&sid=1&ftxt=1

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