A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2

por Huang, Bangqing, Liu, Yanping, Gao, Xue, Xu, Jincao, Dai, Pu, Zhu, Qingwen, Yuan, Yongyi
Publicado 2017

Transcriptomic analysis of mouse cochleae suffering from gentamicin damage reveals the signalling pathways involved in hair cell regeneration

por Bai, Huanju, Jiang, Lingling, Wang, Xi, Gao, Xue, Bing, Jie, Xi, Chao, Wang, Weiqian, Zhang, Meiguang, Zhang, Xinwen, Han, Zhongming, Xu, Jincao, Zeng, Shaoju
Publicado 2019