A Chinese child with hyperpigmentation diagnosed with familial glucocorticoid deficiency type 1 using whole-exome sequencing
Xia, Junke, Jiao, Zhihui, Zhao, Zhenhua, Wu, Jing, Kong, XiangdongJournal:
Pediatrics & Neonatology
DOI:
10.1016/j.pedneo.2020.10.013
Date:
November, 2020
Fichier:
PDF, 297 KB
2020
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