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Extraadrenal 21-Hydroxylation by CYP2C19 and CYP3A4: Effect on 21-Hydroxylase Deficiency

Context: 21-Hydroxylase deficiency (21OHD) is caused by CYP21A2 gene mutations disrupting the adrenal 21-hydroxylase, P450c21. CYP21A2 mutations generally correlate well with the 21OHD phenotype, but some children with severe CYP21A2 mutations have residual 21-hydroxylase activity. Some hepatic P450...

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Detalhes bibliográficos
Main Authors: Gomes, Larissa G., Huang, Ningwu, Agrawal, Vishal, Mendonça, Berenice B., Bachega, Tania A. S. S., Miller, Walter L.
Formato: Artigo
Idioma:Inglês
Publicado em: The Endocrine Society 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2630875/
https://ncbi.nlm.nih.gov/pubmed/18957504
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jc.2008-1174
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