Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

Gao, X., Yuan, Y.-Y., Lin, Q.-F., Xu, J.-C., Wang, W.-Q., Qiao, Y.-H., Kang, D.-Y., Bai, D., Xin, F., Huang, S.-S., Qiu, S.-W., Guan, L.-P., Su, Y., Wang, G.-J., Han, M.-Y., Jiang, Y., Liu, H.-K., Dai, P.
BMJ Publishing Group
Published 2018