The first pediatric case of glucagon receptor defect due to...

Molecular Genetics and Metabolism Reports 2018 / 12 Vol. 17

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

Li, Hong, Zhao, Lihua, Singh, Rani, Ham, J. Nina, Fadoju, Doris O., Bean, Lora J.H., Zhang, Yan, Xu, Yong, Xu, H. Eric, Gambello, Michael J.
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Volume:
17
Language:
english
Journal:
Molecular Genetics and Metabolism Reports
DOI:
10.1016/j.ymgmr.2018.09.006
Date:
December, 2018
File:
PDF, 1.36 MB
english, 2018
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