A review of the literature on common CYP17A1 mutations in adults with 17-hydroxylase/17,20-lyase deficiency, a case series of such mutations among Koreans and functional characteristics of a novel mutation

✍ Scribed by Kim, Yoo-Mi; Kang, Minji; Choi, Jin-Ho; Lee, Beom Hee; Kim, Gu-Hwan; Ohn, Jung Hun; Kim, Seong Yeon; Park, Moon Soo; Yoo, Han-Wook

• Book ID: 124114890
• Publisher: Elsevier Science
• Year: 2014
• Tongue: English
• Weight: 977 KB
• Volume: 63
• Category: Article
• ISSN: 1532-8600
• DOI: 10.1016/j.metabol.2013.08.015