Junction Site Analysis of Chimeric CYP21A1P/CYP21A2 Genes in 21-Hydroxylase Deficiency

BACKGROUND: Chimeric CYP21A1P/CYP21A2 genes, caused by homologous recombination between CYP21A2 (cytochrome P450, family 21, subfamily A, polypeptide 2) and its highly homologous pseudogene CYP21A1P (cytochrome P450, family 21, subfamily A, polypeptide 1 pseudogene), are common in patients with cong...

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Vydáno v:Clin Chem
Hlavní autoři: Chen, Wuyan, Xu, Zhi, Sullivan, Annie, Finkielstain, Gabriela P., Van Ryzin, Carol, Merke, Deborah P., McDonnell, Nazli B.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2011
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5576027/
https://ncbi.nlm.nih.gov/pubmed/22156666
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1373/clinchem.2011.174037
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