ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss
- 期刊名称Human Genetics
- 作者Li, Wu; Sun, Jie; Ling, Jie; Li, Jiada; He, Chufeng; Liu, Yalan; Chen, Hongsheng; Men, Meichao; Niu, Zhijie; Deng, Yuyuan; Li, Meng; Li, Taoxi; Wen, Jie; Sang, Shushan; Li, Haibo; Wan, Zhengqing; Richard, Elodie M.; Chapagain, Prem; Yan, Denise; Liu, Xue Zhong; Mei, Lingyun; Feng, Yong
- 卷第137卷
- 期第4期
- 印刷ISSN0340-6717
- 电子ISSN1432-1203
- 文件大小2499.52KB
- 发表时间2018-4
- DOI10.1007/s00439-018-1885-0
- 页码329-342
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