Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss
干扰素λ受体1（IFNLR1）的突变与常染色体显性遗传性非综合征性听力损失相关。
期刊:Journal of Medical Genetics
影响因子:3.5
doi:10.1136/jmedgenet-2017-104954
Xue Gao #,Yong-Yi Yuan #,Qiong-Fen Lin #,Jin-Cao Xu,Wei-Qian Wang,Yue-Hua Qiao,Dong-Yang Kang,Dan Bai,Feng Xin,Sha-Sha Huang,Shi-Wei Qiu,Li-Ping Guan,Yu Su,Guo-Jian Wang,Ming-Yu Han,Yi Jiang,Han-Kui Liu,Pu Dai
