17α-Hydroxylase Deficiency Diagnosed in Early Infancy Caused by a Novel Mutation of the CYP17A1 Gene

Publisher: Karger

E-ISSN: 1663-2826|81|5|350-355

ISSN: 1663-2818

Source: Hormone Research in Paediatrics, Vol.81, Iss.5, 2014-04, pp. : 350-355

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract