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. |
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| 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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