Homo sapiens mitochondrial 11beta-hydroxylase (CYP11B1) gene, exons 7, - Nucleotide

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[Analysis of a family with 11β-hydroxylase deficiency due to a mutation in the CYP11B1 gene]. [Zhonghua Yi Xue Za Zhi. 2024]
[Analysis of a family with 11β-hydroxylase deficiency due to a mutation in the CYP11B1 gene].
Yu YY, Tao YK, Hou JZ, Zhou GX, Du JJ, Zhang D. Zhonghua Yi Xue Za Zhi. 2024 Jun 11; 104(22):2074-2078.
Identification and functional characterization of compound heterozygous CYP11B1 gene mutations. [Endocrine. 2024]
Identification and functional characterization of compound heterozygous CYP11B1 gene mutations.
Liu H, Liu F, Wei Z, Liu P, Liu Q, Chen L, Hou X. Endocrine. 2024 Apr; 84(1):253-264. Epub 2024 Jan 29.
Clinical and molecular characterization of 10 Chinese children with congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency. [World J Pediatr. 2024]
Clinical and molecular characterization of 10 Chinese children with congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency.
Lu WL, Ma XY, Zhang J, Wang JQ, Zhang TT, Ye L, Xiao Y, Dong ZY, Wang W, Sun SY, et al. World J Pediatr. 2024 Apr; 20(4):422-433. Epub 2023 Jul 24.