Identification of Two Novel Compound Heterozygous EIF2AK3 Mutations Underlying Wolcott–Rallison Syndrome in a Chinese Family

Frontiers in Pediatrics

Yanling Yang¹  Han Xiao²  Changxin Wu²  Na Zhao²  Ping Li²  Qiuhong Xiong² 

[1] Department of Pediatrics, Peking University First Hospital, Beijing, China;Institutes of Biomedical Sciences, Key Laboratory of Chemical Biology and Molecular Engineering of National Ministry of Education, Shanxi University, Taiyuan, China;

关键词: WRS;    EIF2AK3;    PERK;    diabetes;    variation;   

DOI  :  10.3389/fped.2021.679646

来源: Frontiers

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