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

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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, Tadej1,3, 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
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  Data: Clinical Role of CYP2C19 Polymorphisms in Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency.
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  Data: <searchLink fieldCode="JN" term="%22Acta+Chimica+Slovenica%22">Acta Chimica Slovenica</searchLink>. 2016, Vol. 63 Issue 1, p33-37. 5p. 2 Charts.
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        Value: 10.17344/acsi.2015.1797
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        Text: English
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      – TitleFull: Clinical Role of CYP2C19 Polymorphisms in Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency.
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