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

• Những tác giả chính: Marjan MASOUDI (Tác giả), Najmeh AHANGARI (Tác giả), Ali Akbar POURSADEGH ZONOUZI (Tác giả), Ahmad POURSADEGH ZONOUZI (Tác giả), Azim NEJATIZADEH (Tác giả)
• Định dạng: Sách
• Được phát hành: Tehran University of Medical Sciences, 2016-05-01T00:00:00Z.
• Những chủ đề: article
• Truy cập trực tuyến: 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...