Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss

• المؤلفون الرئيسيون: Marjan MASOUDI (مؤلف), Najmeh AHANGARI (مؤلف), Ali Akbar POURSADEGH ZONOUZI (مؤلف), Ahmad POURSADEGH ZONOUZI (مؤلف), Azim NEJATIZADEH (مؤلف)
• التنسيق: كتاب
• منشور في: Tehran University of Medical Sciences, 2016-05-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Background: Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common hereditary form of deafness, and exhibits a great deal of genetic heterogeneity. So far, more than seventy various DFNB loci have been mapped for ARNSHL by linkage analysis. The contribution of three common DFNB l...