Fernandes-Rosa, F. L., de Castro, M., Latronico, A. C., Sippell, W. G., Riepe, F. G., & Antonini, S. R. (2006). Recurrence of the R947X Mutation in Unrelated Families with Autosomal Dominant Pseudohypoaldosteronism Type 1: Evidence for a Mutational Hot Spot in the Mineralocorticoid Receptor Gene. The journal of clinical endocrinology and metabolism, 91(9), 3671-3675. https://doi.org/10.1210/jc.2006-0605
Chicago Style (17th ed.) CitationFernandes-Rosa, Fabio L., Margaret de Castro, Ana Claudia Latronico, Wolfgang G. Sippell, Felix G. Riepe, and Sonir R. Antonini. "Recurrence of the R947X Mutation in Unrelated Families with Autosomal Dominant Pseudohypoaldosteronism Type 1: Evidence for a Mutational Hot Spot in the Mineralocorticoid Receptor Gene." The Journal of Clinical Endocrinology and Metabolism 91, no. 9 (2006): 3671-3675. https://doi.org/10.1210/jc.2006-0605.
MLA (9th ed.) CitationFernandes-Rosa, Fabio L., et al. "Recurrence of the R947X Mutation in Unrelated Families with Autosomal Dominant Pseudohypoaldosteronism Type 1: Evidence for a Mutational Hot Spot in the Mineralocorticoid Receptor Gene." The Journal of Clinical Endocrinology and Metabolism, vol. 91, no. 9, 2006, pp. 3671-3675, https://doi.org/10.1210/jc.2006-0605.