Familial neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin II gene.

MLA

de Fost, M., et al. “Familial Neurohypophyseal Diabetes Insipidus Due to a Novel Mutation in the Arginine Vasopressin-Neurophysin II Gene.” European Journal of Endocrinology, vol. 165, no. 1, July 2011, pp. 161–65. EBSCOhost, https://doi.org/10.1530/EJE-11-0048.

APA

de Fost, M., van Trotsenburg, A. S. P., van Santen, H. M., Endert, E., van den Elzen, C., Kamsteeg, E. J., Swaab, D. F., & Fliers, E. (2011). Familial neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin II gene. European Journal of Endocrinology, 165(1), 161–165. https://doi.org/10.1530/EJE-11-0048

Chicago

de Fost, M, A S P van Trotsenburg, H M van Santen, E Endert, C van den Elzen, E J Kamsteeg, D F Swaab, and E Fliers. 2011. “Familial Neurohypophyseal Diabetes Insipidus Due to a Novel Mutation in the Arginine Vasopressin-Neurophysin II Gene.” European Journal of Endocrinology 165 (1): 161–65. doi:10.1530/EJE-11-0048.