Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: MedlinePlus Genetics
CYP11B1 Gene - GeneCards | C11B1 Protein | C11B1 Antibody
Novel mutations in the CYP11B2 gene causing aldosterone synthase deficiency
Characterisation of three novel CYP11B1 mutations in classic and non-classic 11β-hydroxylase deficiency in: European Journal of Endocrinology Volume 170 Issue 5 (2014)
Preclinical diagnosis and identification of the chimeric CYP11B1/CYP11B2 gene in two pediatric cases of a Japanese family with glucocorticoid-remediable aldosteronism | Hypertension Research
GENETICS IN ENDOCRINOLOGY: The expanding genetic horizon of primary aldosteronism in: European Journal of Endocrinology Volume 178 Issue 3 (2018)
Figure 1 from A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy | Semantic Scholar
Development of CYP11B1 and CYP11B2 assays utilizing homogenates of adrenal glands: Utility of monkey as a surrogate for human - ScienceDirect
A Novel Mutation in the CYP11B1 Gene Causes Steroid 11β-Hydroxylase Deficient Congenital Adrenal Hyperplasia with Reversible Cardiomyopathy
Frontiers | Detection of Small CYP11B1 Deletions and One Founder Chimeric CYP11B2/CYP11B1 Gene in 11β-Hydroxylase Deficiency
CYP11B1 Antibody (NBP1-68883): Novus Biologicals
Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency | PNAS
Associations Between Human Aldosterone Synthase (CYP11B2) Gene Polymorphisms and Left Ventricular Size, Mass, and Function | Circulation
CYP11B1 gene and localization of the novel mutation are shown... | Download Scientific Diagram
Aldosterone Synthase - an overview | ScienceDirect Topics
Development of CYP11B1 and CYP11B2 assays utilizing homogenates of adrenal glands: Utility of monkey as a surrogate for human - ScienceDirect
Recombinant gametes formed by unequal crossing over between the CYP11B1... | Download Scientific Diagram
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations | European Journal of Human Genetics
IJMS | Free Full-Text | Molecular and Epigenetic Control of Aldosterone Synthase, CYP11B2 and 11-Hydroxylase, CYP11B1
Frontiers | Clinical and Molecular Analysis of Four Patients With 11β-Hydroxylase Deficiency
CYP11B structure of the patient. A chimeric CYP11B2/CYP11B1 lies in one... | Download Scientific Diagram
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: description of a new mutation, R384X
Genetic organization of CYP11b1 gene illustrates DNA sequence... | Download Scientific Diagram
A, Sequence analysis showing CYP11B1, CYP11B2, and the CYP11B1/ CYP11B2... | Download Scientific Diagram
Common Polymorphisms in the CYP11B1 and CYP11B2 Genes: Evidence for a Digenic Influence on Hypertension | Hypertension
CYP11B1 Gene - GeneCards | C11B1 Protein | C11B1 Antibody
CYP11B1 Gene - GeneCards | C11B1 Protein | C11B1 Antibody
Structure of the human CYP11B1 gene with the pathogenic variants that... | Download Scientific Diagram
