转导蛋白β样1X基因与迟发性感音神经性耳聋
An overview on transducin beta like 1 X-linked gene and delayed sensorineural hearing loss
王艳莉 1郭玉芬1
作者信息
- 1. 兰州大学第二医院耳鼻咽喉头颈外科(兰州 730000)
- 折叠
摘要
目前的研究表明,人源转导蛋白β样1X(transducin beta like 1 X-linked,TBL1X)基因与多种疾病的发生密切相关,还参与了迟发性感音神经性耳聋的发生,我们回顾国内外的相关文献,就该基因与迟发性感音神经性耳聋的相关研究做一综述.
Abstract
Current studies have shown that the TBL1X gene is closely related to the occurrence of multiple diseas-es,and is also involved in the occurrence of delayed sensorineural hearing loss.This paper reviews relevant literatures published both at home and abroad,particularly studies on the relationship between this gene and delayed sensorineural hearing loss.
关键词
人源转导蛋白β样1X基因/眼白化病/中枢性甲状腺功能减退/迟发感音神经性耳聋Key words
transducin beta like 1 X-linked(TBL1X)gene/ocular albinism/central hypothyroidism/delayed sen-sorineural hearing loss引用本文复制引用
基金项目
国家自然科学基金地区基金项目(82360221)
出版年
2024
国家科技期刊平台
NSTL
万方数据