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NKX2-1在先天性甲状腺功能减退中的功能研究 被引量：1

Functional study of NKX2-1 in congenital hypothyroidism
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摘要 分析了先天性甲状腺功能减退病因学及引致原因,阐述了N2.KX2-1基因表达异常引起甲状腺受累的具体表现,对NKX2-1在先天性甲状腺功能减退中的功能研究进展进行探究,旨意为分析NKX2-1在先天性甲状腺功能减退中的功能的相关研究提供参考文献。 The etiology and causes of congenital hypothyroidism were analyzed.The specific manifestations of abnormal thyroid involvement caused by abnormal expression of N2.KX2-1 gene were described.The function of NKX2-1 in congenital hypothyroidism was explored.The purpose of this study is to provide a reference for the study of the function of NKX2-1 in congenital hypothyroidism.
作者 顾斌洁 GU Bin-jie(College of Life Sciences,Central China Normal University,Wuhan 430079,China)
机构地区 华中师范大学生命科学学院
出处 《黑龙江科学》 2018年第5期88-89,共2页 Heilongjiang Science
关键词 NKX2-1基因 先天性甲状腺功能减退 基因突变 NKX2-1 gene Congenital hypothyroidism Gene mutation
分类号 R722.1 [医药卫生—儿科]
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黑龙江科学
2018年 第5期

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