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File Title: The first pediatric case of glucagon receptor defect due to biallelic mutations in GCGR is identified by newborn screening of elevated arginine
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User eporter@emory.edu has attached Publication File - tdth6.pdf to The first pediatric case of glucagon receptor defect due to biallelic mutations in GCGR is identified by newborn screening of elevated arginine March 20th, 2025 07:24
User eporter@emory.edu has deposited Publication File - tdth6.pdf March 20th, 2025 07:23