Clinical Role of CYP2C19 Polymorphisms in Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency.

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Bibliographic Details
Title:	Clinical Role of CYP2C19 Polymorphisms in Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency.
Authors:	Grošelj, Urh¹, Tanšek, Mojca Žerjav¹, Podkrajšek, Katarina Trebušak², Hovnik, Tinka², Battelino, Tadej^1,3, Dolžan, Vita⁴ vita.dolzan@mf.uni-lj.si
Source:	Acta Chimica Slovenica. 2016, Vol. 63 Issue 1, p33-37. 5p. 2 Charts.
Database:	Academic Search Ultimate

Description
ISSN:	13180207
DOI:	10.17344/acsi.2015.1797