Nobel, Y. R., Lodish, M. B., Raygada, M., Del Rivero, J., Faucz, F. R., Abraham, S. B., . . . Zilbermint, M. (2016). Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene. Endocrinol Diabetes Metab Case Rep.
Chicago-stil citatNobel, Yael R., et al. "Pseudohypoaldosteronism Type 1 Due to Novel Variants of SCNN1B Gene." Endocrinol Diabetes Metab Case Rep 2016.
MLA-referensNobel, Yael R., et al. "Pseudohypoaldosteronism Type 1 Due to Novel Variants of SCNN1B Gene." Endocrinol Diabetes Metab Case Rep 2016.
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