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Steroid 11β-hydroxylase deficiency and related disorders
Perrin C. White
Pediatrics
Endocrinology
Research output
:
Chapter in Book/Report/Conference proceeding
›
Chapter
2
Scopus citations
Overview
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Keyphrases
Related Disorders
100%
11β-hydroxylase Deficiency
100%
Deficiency Diseases
100%
Deoxycorticosterone
75%
Cortisol
50%
CYP11B2
50%
Autosomal Dominant
25%
Polymorphism
25%
Hypertension
25%
Isozymes
25%
Angiotensin II (Ang II)
25%
Hypovolemia
25%
Hyponatremia
25%
Hydroxylase
25%
Congenital Adrenal Hyperplasia
25%
Hypertension Risk
25%
Aldosterone
25%
Hyperkalemia
25%
Corticosterone
25%
Aldosterone Synthase
25%
Aldosterone Secretion
25%
Aldosterone Synthesis
25%
CYP11B1 Gene
25%
CYP11B1
25%
CYP11B
25%
Hyperaldosteronism
25%
Chimeric Gene
25%
Unequal Crossing over
25%
Potassium Levels
25%
Recessive Disorder
25%
Oxidase Activity
25%
Aldosterone Synthase Deficiency
25%
Biochemistry, Genetics and Molecular Biology
Oxygenase
100%
Aldosterone Synthase
80%
Cortisol
40%
Aldosterone
40%
Oxidoreductase
20%
Enzyme
20%
Autosomal Dominant Inheritance
20%
Adrenocorticotropic Hormone
20%
Isozyme
20%
Glucocorticoid
20%
Angiotensin
20%
Oxidase
20%
Cortodoxone
20%
Infancy
20%
Corticosterone
20%
Aldosterone Release
20%
Chimeric Gene
20%
Unequal Crossing over
20%
11-Deoxycorticosterone
20%
Hyponatremia
20%
Hyperkalemia
20%