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21 Hydroxylase
(compound)
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Genetic Markers
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Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
Tet1 hydroxylase knockdown in embryonic stem cells
Cardiomyocytes with OGFOD1 knockout treated with dimethyloxalylglycine
Liver tissue from CYP7A1 transgenic mice fed with high fat high cholesterol Western diet
Gender-specific liver and heart expression responses to PPAR-alpha
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Literature
Most Relevant Literature
Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-h…
Why human cytochrome P450c21 is a progesterone 21-hydroxylase.
The purification and application of biologically active recombinant steroid cytochrome P450 21-hydro…
T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adren…
The frequency of 21-alpha hydroxylase enzyme deficiency and related sex hormones in Iraqi healthy ma…
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Clinical Trials
Most Relevant Clinical Trials
Adrenocortical Functions in Women With Nonclassical 21-hydroxylase Deficiency.
A Study Examining Doses of Abiraterone Acetate in Adult Women With 21-Hydroxylase Deficiency
Examining Genetic Differences Among People With 21-Hydroxylase Deficiency
Determining the Long-Term Effects of Prenatal Dexamethasone Treatment in Children With 21-Hydroxylas…
Tyrosine Hydroxylase Antibody Levels in Autoimmune Polyglandular Syndrome Type 1 Associated Keratiti…
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