The association of genetic polymorphisms in interleukin-1 receptors type 1 and type 2 with sudden sensorineural hearing loss in a Taiwanese population: a case control study.
Chen-Yu ChienShu-Yu TaiKuan-Hui LiHua-Ling YangLeong-Perng ChanEdward HsiLing-Feng WangKuen-Yao HoNing-Chia ChangPublished in: Journal of otolaryngology - head & neck surgery = Le Journal d'oto-rhino-laryngologie et de chirurgie cervico-faciale (2021)
These findings suggest that IL1R1 and IL1R2 gene polymorphisms may contribute to an increased risk of SSNHL in Taiwan.
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