Construction of Wild Type and Mutant ATP6V1B2 Ggene Vector and Preliminary Study on Function of ATP6V1B2 MutationXIN Feng, YUAN Yong-yi, GUO Wei-wei, Han Dongyi, DAI Pu335-339
Whole Exome Sequencing Identifies ACTG1 as the Mutated Gene in a Chinese Family with Autosomal Dominant Non-Syndromic Hearing LossLU Yu, ZHANG Xu, YAN Zhi-Qiang, WANG Yan-Fei, ZHENG Long-Yan, GUO Fei-Fei, CHENG Jing, HAN Dong-Yi, Chen Xiao-Wei, YUAN Hui-Jun340-344
Mechanism and Functional Research on Nuclear Modified Gene Associated with Maternally Inherited Aminoglycoside-Induced DeafnessLiu Ri-yuan, Liu Qi, Hao Qing-qing, Dong Si-qi, Xu Guang-yu, Zhao Hui345-352
Preservation of Residual Hearing after Minimally Invasive Cochlear ImplantationWANG Cui-cui, DAI Pu, HAN Dong-yi375-379
An Clinical Research on Newborn Hearing Concurrent Genetic Screening in 106,513 NeonatesHAN Bing, LI Qian, ZONG Liang, LAN Lan, ZHAO Ya-li, WANG Da-yong, ZHAO Cui, LIU Nan, GUAN Jing, WANG Qiu-ju380-383
Strategy of prevention and therapeutics against sensorineural hearing Loss via local application to inner earXIA Li, YIN Shan-kai401-407
Assessment of Auditory Function in Children with Obstructive Sleep Apnea-Hypopnea SyndromeZhang Xiao-hui, Sun Xiao-ping, Xu Zhao-xia, Guo Ai-ping, Yang Jing-li418-422
Factors Affecting Quality of Life after Endolymphatic Sac SurgeryHAN LIn, YU Li-sheng, LIU Yan, XIA Yui-ming423-427