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6 Molecular genetics of congenital adrenal hyperplasia
Perrin C. White
, Maria I. New
Pediatrics
Endocrinology
Research output
:
Contribution to journal
›
Article
›
peer-review
19
Scopus citations
Overview
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Medicine & Life Sciences
Congenital Adrenal Hyperplasia
100%
Molecular Biology
61%
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency
61%
Mixed Function Oxygenases
60%
Steroid 21-Hydroxylase
47%
Cytochrome P-450 Enzyme System
31%
Steroid 17-alpha-Hydroxylase
31%
Genes
30%
Pseudogenes
27%
3-Hydroxysteroid Dehydrogenases
18%
Enzymes
17%
Chromosomes
17%
Cholesterol Side-Chain Cleavage Enzyme
16%
Alleles
15%
Chromosomes, Human, Pair 15
14%
Gene Conversion
14%
Chromosomes, Human, Pair 10
14%
Mitochondrial Genes
13%
Mutation
12%
Major Histocompatibility Complex
11%
Adrenocorticotropic Hormone
10%
Introns
10%
Cluster Analysis
9%
Hydrocortisone
9%
Exons
9%
Cholesterol
7%
Chemical Compounds
Cholesterol
67%
Mutation
63%
Cortisol
48%
Cytochrome P450
40%