Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness

ConclusionOur results expanded the mutation spectrum and genotype ‒phenotype correlation of nonsyndromic hearing loss in Chinese Hans and also emphasized the importance of combining both next‐generation sequencing and detailed auditory evaluation to achieve a more accurate diagnosis for nonsyndromic hearing loss.

Source: Molecular Genetics & Genomic Medicine - February 13, 2020 Category: Genetics & Stem Cells Authors: Di Wu, Weiyuan Huang, Zhenhang Xu, Shuo Li, Jie Zhang, Xiaohua Chen, Yan Tang, Jinhong Qiu, Zhixia Wang, Xuchu Duan, Luping Zhang Tags: CLINICAL REPORT Source Type: research