Low frequency of SLC26A4 c.919-2A   >  G variant among patients with nonsyndromic hearing loss in Yunnan of Southwest China

Gene variants are responsible for more than half of hearing loss, particularly in nonsyndromic hearing loss (NSHL). The most common pathogenic variant in SLC26A4 gene found in East Asian populations is c.919-2A  >...

Source: BMC Medical Genomics - February 20, 2024 Category: Genetics & Stem Cells Authors: Yan-Qiong Li, Heng Ma, Qin-Yao Wang, De-Sheng Liu, Wei Wang, Shi-Xin Li, Rong-Xia Zuo, Tao Shen, Bao-Sheng Zhu and Ya-Lian Sa Tags: Research Source Type: research