Title : A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutism.

Pub. Date : 2013 Oct

PMID : 23940125






1 Functional Relationships(s)
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1 Novel CYP11B1 mutations were functionally analyzed in transiently transfected COS7 cells measuring the conversion of 11-deoxycortisol to cortisol by liquid chromatography-tandem mass spectrometry. Hydrocortisone cytochrome P450 family 11 subfamily B member 1 Homo sapiens