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The first pediatric case of glucagon receptor defect due to biallelic mutations in GCGR is identified by newborn screening of elevated arginine

Authors:Hong Li, Emory UniversityLihua Zhao, Chinese Academy of SciencesRani Singh, Emory UniversityJee-Young Ham, Emory UniversityDoris O. Fadoju, Emory UniversityLora H Bean, Emory UniversityYan Zhang, Chinese Academy of SciencesYong Xu, Chinese Academy of SciencesH. Eric Xu, Chinese Academy of SciencesMichael Gambello, Emory University

Date:2018

Publisher:Elsevier

Publication Version:Final Published Version

License:Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International