Clinical Role of CYP2C19 Polymorphisms in Patients with Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency. - Grošelj, Urh; Tanšek, Mojca Žerjav; Podkrajšek, Katarina Trebušak; Hovnik, Tinka; Battelino, Tadej; Dolžan, Vita (Acta Chimica Slovenica, 2016)