Clinical and HSD11B2 gene analysis of a patient with apparent mineralocorticoid excess.

Author: Yuan DING ¹ ; Xiao Qiao LI ¹ ; Xue Jun LIANG ¹ ; Chun Xiu GONG ¹
Author Information

1. Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Publication Type:Journal Article
MeSH: 11-beta-Hydroxysteroid Dehydrogenase Type 2/genetics*; Humans; Mineralocorticoid Excess Syndrome, Apparent/genetics*; Pedigree
From: Chinese Journal of Pediatrics 2022;60(5):468-470
CountryChina
Language:Chinese