Distinctive profile of the 17-hydroxylase and 17,20-lyase activities revealed by urinary steroid metabolomes of patients with CYP17 deficiency.
about
A missense mutation in the human cytochrome b5 gene causes 46,XY disorder of sex development due to true isolated 17,20 lyase deficiencyThe hunt for a selective 17,20 lyase inhibitor; learning lessons from nature.Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency
P2860
Distinctive profile of the 17-hydroxylase and 17,20-lyase activities revealed by urinary steroid metabolomes of patients with CYP17 deficiency.
description
2010 nî lūn-bûn
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2010年の論文
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2010年論文
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2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
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2010年論文
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2010年论文
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2010年论文
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name
Distinctive profile of the 17- ...... atients with CYP17 deficiency.
@en
Distinctive profile of the 17- ...... atients with CYP17 deficiency.
@nl
type
label
Distinctive profile of the 17- ...... atients with CYP17 deficiency.
@en
Distinctive profile of the 17- ...... atients with CYP17 deficiency.
@nl
prefLabel
Distinctive profile of the 17- ...... atients with CYP17 deficiency.
@en
Distinctive profile of the 17- ...... atients with CYP17 deficiency.
@nl
P2093
P2860
P1476
Distinctive profile of the 17- ...... atients with CYP17 deficiency.
@en
P2093
Cedric H L Shackleton
Claudio E Kater
Marcos S Neres
Richard J Auchus
P2860
P304
P356
10.1590/S0004-27302010000900009
P577
2010-12-01T00:00:00Z