Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H2O2 Generation-Reference-Cited by-同舟云学术

Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H2O2 Generation

Published:2019-08-02 Issue: Volume:10 Page:
ISSN:1664-2392
Container-title:Frontiers in Endocrinology
language:
Short-container-title:Front. Endocrinol.

Author:

Liu Shiguo,Han Wenxiu,Zang Yucui,Zang Hongwei,Wang Fang,Jiang Pei,Wei Hongwei,Liu Xiangju,Wang Yangang,Ma Xu,Ge Yinlin

Funder

National Natural Science Foundation of China

National Basic Research Program of China (973 Program)

Publisher

Frontiers Media SA

Subject

Endocrinology, Diabetes and Metabolism

Reference31 articles.

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