| 注册
首页|期刊导航|中华耳科学杂志|转导蛋白β样1X基因与迟发性感音神经性耳聋

转导蛋白β样1X基因与迟发性感音神经性耳聋

王艳莉 郭玉芬

中华耳科学杂志2024,Vol.22Issue(4):671-673,3.
中华耳科学杂志2024,Vol.22Issue(4):671-673,3.DOI:10.3969/j.issn.1672-2922.2024.04.028

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

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

王艳莉,郭玉芬..转导蛋白β样1X基因与迟发性感音神经性耳聋[J].中华耳科学杂志,2024,22(4):671-673,3.

基金项目

国家自然科学基金地区基金项目(82360221) (82360221)

中华耳科学杂志

OA北大核心CSTPCD

1672-2922

访问量5
|
下载量0
段落导航相关论文