Mutation of IFNLR1 , an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss
Gao, Xue, Yuan, Yong-Yi, Lin, Qiong-Fen, Xu, Jin-Cao, Wang, Wei-Qian, Qiao, Yue-Hua, Kang, Dong-Yang, Bai, Dan, Xin, Feng, Huang, Sha-Sha, Qiu, Shi-Wei, Guan, Li-Ping, Su, Yu, Wang, Guo-Jian, Han, MinLanguage:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2017-104954
Date:
February, 2018
File:
PDF, 2.77 MB
english, 2018