bibliographicCitation |
Løvås K, McFarlane I, Nguyen HH, Curran S, Schwabe J, Halsall D, Bernhardt R, Wallace AM, Chatterjee VK. A novel CYP11B2 gene mutation in an Asian family with aldosterone synthase deficiency. J Clin Endocrinol Metab. 2009 Mar;94(3):914–9. doi: 10.1210/jc.2008-1524. PMID: 19116236. |