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

• Hauptverfasser: Yan-Qiong Li (Verfasst von), Heng Ma (Verfasst von), Qin-Yao Wang (Verfasst von), De-Sheng Liu (Verfasst von), Wei Wang (Verfasst von), Shi-Xin Li (Verfasst von), Rong-Xia Zuo (Verfasst von), Tao Shen (Verfasst von), Bao-Sheng Zhu (Verfasst von), Ya-Lian Sa (Verfasst von)
• Format: Buch
• Veröffentlicht: BMC, 2024-02-01T00:00:00Z.
• Schlagworte: article
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Abstract Background 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 > G followed by c.2168A > G (p.H723R). This study was to evalua...