000 01090 a2200313 4500
005 20250518000104.0
264 0 _c20181211
008 201812s 0 0 eng d
022 _a1757-2215
024 7 _a10.1186/s13048-018-0450-8
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aWang, Dongdong
245 0 0 _aNon-classical 11β-hydroxylase deficiency caused by compound heterozygous mutations: a case study and literature review.
_h[electronic resource]
260 _bJournal of ovarian research
_cSep 2018
300 _a82 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article; Review
650 0 4 _aAdrenal Hyperplasia, Congenital
_xblood
650 0 4 _aAdult
650 0 4 _aFemale
650 0 4 _aHumans
650 0 4 _aMutation
650 0 4 _aSteroid 11-beta-Hydroxylase
_xblood
650 0 4 _aYoung Adult
700 1 _aWang, Jiahui
700 1 _aTong, Tong
700 1 _aYang, Qing
773 0 _tJournal of ovarian research
_gvol. 11
_gno. 1
_gp. 82
856 4 0 _uhttps://doi.org/10.1186/s13048-018-0450-8
_zAvailable from publisher's website
999 _c28843887
_d28843887