Non-classical 11β-hydroxylase deficiency caused by compound heterozygous mutations: a case study and literature review.

Wang, Dongdong

Non-classical 11β-hydroxylase deficiency caused by compound heterozygous mutations: a case study and literature review. [electronic resource] - Journal of ovarian research Sep 2018 - 82 p. digital

Publication Type: Case Reports; Journal Article; Review

1757-2215

10.1186/s13048-018-0450-8 doi


Adrenal Hyperplasia, Congenital--blood
Adult
Female
Humans
Mutation
Steroid 11-beta-Hydroxylase--blood
Young Adult