Distinctive profile of the 17-hydroxylase and 17,20-lyase activities revealed by urinary steroid metabolomes of patients with CYP17 deficiency

Article

Abstract: Objectives: (1) Characterize serum (S) and urinary (U) steroid metabolites in complete CYP17 deficie

Palabras claves:

17, 17-hydroxylase deficiency, 20-lyase deficiency, Congenital adrenal hyperplasia, Corticosterone, CYP17, Urinary steroid metabolome

Autores:

Kater C.E., Neres M.S., Richard J. Auchus, Shackleton C.H.L.

Fuentes:

scopus