Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder

por Tang, Fengzhu, Ma, Dengke, Wang, Yulan, Qiu, Yuecai, Liu, Fei, Wang, Qingqing, Lu, Qiutian, Shi, Min, Xu, Liang, Liu, Min, Liang, Jianping
Publicado 2017

A novel SLC26A4 splicing mutation identified in two deaf Chinese twin sisters with enlarged vestibular aqueducts

por Zhou, Kai, Huang, Lancheng, Feng, Menglong, Li, Xinlei, Zhao, Yi, Liu, Fei, Wei, Jiazhang, Qin, Danxue, Lu, Qiutian, Shi, Min, Qu, Shenhong, Tang, Fengzhu
Publicado 2020