A Chinese patient with 11β-hydroxylase deficiency due to novel compound heterozygous mutation in CYP11B1 gene: a case report
Yuan, Xianxian, Lu, Lin, Chen, Shi, Jiang, Jun, Wang, Xiangqing, Liu, Zhihui, Zhu, Huijuan, Pan, Hui, Lu, ZhaolinVolume:
18
Langue:
english
Journal:
BMC Endocrine Disorders
DOI:
10.1186/s12902-018-0295-6
Date:
December, 2018
Fichier:
PDF, 2.44 MB
english, 2018