Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital Hypothyroidism

Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital Hypothyroidism

INTRODUCTION: Defects in the human solute carrier family 26 member 4 (SLC26A4) gene are reported to be one of the causes of congenital hypothyroidism (CH). We aimed to identify SLC26A4 mutations in Chinese patients with CH and analyze the function of the mutations. METHODS: Patients with primary CH...

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Bibliographic Details
Main Authors: Chang-Run Zhang, Yuan-Ping Shi, Cao-Xu Zhang, Feng Sun, Wen-Jiao Zhu, Rui-Jia Zhang, Ya Fang, Qian-Yue Zhang, Chen-Yan Yan, Ying-Xia Ying, Shuang-Xia Zhao, Huai-Dong Song
Format: Article
Language:English
Published: Galenos Yayincilik 2022-03-01
Series:JCRPE
Subjects:
congenital hypothyroidism
next-generation sequencing
slc26a4
cell location
ion transport
Online Access:https://jag.journalagent.com/z4/download_fulltext.asp?pdir=jcrpe&un=JCRPE-88598

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https://jag.journalagent.com/z4/download_fulltext.asp?pdir=jcrpe&un=JCRPE-88598

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