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A Chinese child with hyperpigmentation diagnosed with familial glucocorticoid deficiency type 1 using whole-exome sequencing

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Bibliographic Details
Main Authors:	Junke Xia (Author), Zhihui Jiao (Author), Zhenhua Zhao (Author), Jing Wu (Author), Xiangdong Kong (Author)
Format:	Book
Published:	Elsevier, 2021-03-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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