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CYP21A2
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CYP21A2

CYP21A2
See 21-Hydroxylase
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Last updated on Wednesday March 07, 2007 at 09:10:37 PST (GMT -0800)
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Related Articles
A Simple and Robust Quantitative PCR Assay to Determine CYP21A2 Gene Dose in the Diagnosis of 21-Hydroxylase Deficiency
Sep 01, 2007; Background: Correct diagnosis of 21-hydroxylase deficiency (21OHD) requires the identification of CYP21A2 gene deletions...
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Genotyping of CYP21A2 for Congenital Adrenal Hyperplasia Screening using Allele-Specific Primer Extension followed by Bead Array Hybridization
Dec 01, 2009; Background Congenital adrenal hyperplasia (CAH) is an autosomal recessive disease caused by mutations in genes encoding the...
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Multiplex Ligation-Dependent Probe Amplification Analysis Is Useful for Diagnosing Congenital Adrenal Hyperplasia but Requires a Deep Knowledge of CYP21A2 Genetics
Jun 30, 2012; To the Editor: We read with great interest the recent report in Clinical Chemistry by Canturk et al. (1 ). These authors affirmed...
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Junction Site Analysis of Chimeric CYP21A1P/ CYP21A2 Genes in 21-Hydroxylase Deficiency
Feb 01, 2012; BACKGROUND: Chimeric CYP21A1P/CYP21A2 genes, caused by homologous recombination between CYP21A2 (cytochrome P450,...
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C4B null alleles are not associated with genetic polymorphisms in the adjacent gene CYP21A2 in autism.(Research article)(cytochrome P450, family 21, subfamily A, polypeptide 2)
Jan 07, 2008; Authors: Thayne L Sweeten [1]; Daniel W Odell [1,2]; J Dennis Odell [1]; Anthony R Torres (corresponding author) [1] Background...
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