https://blogs.bmj.com/jmg/2018/02/16/mutation-of-ifnlr1-an-interferon-lambda-receptor-1-is-associated-with-autosomal-dominant-non-syndromic-hearing-loss/
Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant...
Feb 24, 2026 - Hearing loss is a common sensory defect that can significantly impact quality of life. The majority of congenital cases are attributable to genetic factors. To...