A Novel NR0B1 Gene Mutation Causes Different Phenotypes in Two Male Patients with Congenital Adrenal Hypoplasia
Crossref DOI link: https://doi.org/10.1007/s11596-020-2161-9
Published Online: 2020-03-13
Published Print: 2020-02
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Wu, Shi-min
Gao, Jin-zhi
He, Bin
Long, Wen-jun
Luo, Xiao-ping
Chen, Ling
Text and Data Mining valid from 2020-02-01
Version of Record valid from 2020-02-01
Article History
Received: 2 May 2019
Revised: 8 December 2019
First Online: 13 March 2020