共 50 条
- [1] Detection of Small CYP11B1 Deletions and One Founder Chimeric CYP11B2/CYP11B1 Gene in 11β-Hydroxylase Deficiency [J]. FRONTIERS IN ENDOCRINOLOGY, 2022, 13
- [3] The human steroid hydroxylases CYP11B1 and CYP11B2 [J]. BIOLOGICAL CHEMISTRY, 2002, 383 (10) : 1537 - 1551
- [4] POINT MUTATIONS IN CYP11B1 CAUSING STEROID 11-BETA-HYDROXYLASE DEFICIENCY [J]. CLINICAL RESEARCH, 1992, 40 (02): : A310 - A310
- [5] Unequal crossing over between CYP11B2 and CYP11B1 causes 11 β -hydroxylase deficiency in a consanguineous family [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2023, 233
- [6] Case Report: A combination of chimeric CYP11B2/CYP11B1 and a novel p.Val68Gly CYP11B1 variant causing 11β-Hydroxylase deficiency in a Chinese patient [J]. FRONTIERS IN ENDOCRINOLOGY, 2023, 14
- [9] Flavone regulation of steroidogenic CYP11B1 and CYP11B2 genes [J]. TOXICOLOGY LETTERS, 2010, 196 : S57 - S58