A Chinese child with hyperpigmentation diagnosed with familial glucocorticoid deficiency type 1 using whole-exome sequencing
Junke Xia,
Zhihui Jiao,
Zhenhua Zhao,
Jing Wu,
Xiangdong Kong
Affiliations
Junke Xia
Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, Zhengzhou, China
Zhihui Jiao
Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, Zhengzhou, China
Zhenhua Zhao
Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, Zhengzhou, China
Jing Wu
Department of Pediatrics, Zhengzhou University First Affiliated Hospital, Zhengzhou, China
Xiangdong Kong
Corresponding author. Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, 1 Jianshe Road, Erqi District, Zhengzhou, 450052, China.; Center of Genetic and Prenatal Diagnosis, Zhengzhou University First Affiliated Hospital, Zhengzhou, China
