Whole-exome sequencing identifies genetic variants of hearing loss in 113 Chinese families

作者：Jianyan Pan, Shanshan Ma, Yanling Teng, Desheng Liang, Zhuo Li, Lingqian Wu · 发表于：Clinica Chimica Acta · 年份：2022 · DOI：10.1016/j.cca.2022.05.020 · 被引用次数：11 · 研究领域：Hearing, Cochlea, Tinnitus, Genetics、Genomics and Rare Diseases、Genetic Neurodegenerative Diseases