A multiplex PCR amplicon sequencing assay to screen genetic hearing loss variants in newborns

• Glavni autori: Haiyan Yang (Autor), Hongyu Luo (Autor), Guiwei Zhang (Autor), Junqing Zhang (Autor), Zhiyu Peng (Autor), Jiale Xiang (Autor)
• Format: Knjiga
• Izdano: BMC, 2021-02-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

Abstract Background Congenital hearing loss is one of the most common birth defects. Early identification and management play a crucial role in improving patients' communication and language acquisition. Previous studies demonstrated that genetic screening complements newborn hearing screening...