Mutation Screening and Functional Study of <i>SLC26A4</i> in Chinese Patients with Congenital Hypothyroidism-Reference-Cited by-同舟云学术

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

Published:2021-09-21 Issue:0 Volume:0 Page:0-0
ISSN:1308-5727
Container-title:Journal of Clinical Research in Pediatric Endocrinology
language:
Short-container-title:Jcrpe

Author:

Zhang Chang-Run,Shi Yuan-Ping,Zhang Cao-Xu,Sun Feng,Zhu Wen-Jiao,Zhang Rui-Jia,Fang Ya,Zhang Qian-Yue,Yan Chen-Yan,Ying Ying-Xia,Zhao Shuang-Xia,Song Huai-Dong

Publisher

Galenos Yayinevi

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The molecular principles underlying diverse functions of the SLC26 family of proteins;Journal of Biological Chemistry;2024-05

2. The molecular principles underlying diverse functions of the SLC26 family of proteins;2023-12-10

3. Asymmetric pendrin homodimer reveals its molecular mechanism as anion exchanger;Nature Communications;2023-05-25

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